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Threatened miscarriage is manifested by vaginal bleeding, with or without abdominal pain, while the cervix is closed and the fetus is viable and inside the uterine cavity. Threatened miscarriage is a common complication of pregnancy occurring in 20% of all clinically recognized pregnancies and about half of these will eventually result in pregnancy loss. The goal of this two by two factorial, placebo controlled randomized trial is to determine that two oral medications and their combination, will mostly likely result in live birth in women with threatened miscarriage. We will evaluate the efficacy and safety of Chinese herbal medicine (New "Shoutai Wan", NSTW) and/or oral micronized progesterone (OP) for treating threatened miscarriage in this trial. Our primary outcome of this trial is live birth. We hypothesize that: 1. treatment with NSTW plus OP or OP placebo is more likely to result in live birth than NSTW placebo plus OP or placebo; 2. treatment with OP plus NSTW or NSTW placebo is more likely to result in live birth than OP placebo plus NSTW or NSTW placebo; 3. treatment with combination of NSTW and OP is more likely to result in live birth than combination of NSTW placebo and OP placebo.
The causes of spontaneous miscarriage are diverse and comprise chromosomal, genetic, anatomical, immunological, hormonal, infectious and psychological factors, the other factors contribute to an increased risk include advancing paternal and maternal age and mothers with systemic diseases, such as diabetes or thyroid dysfunction. The incidence is difficult to determine precisely because it occurs very early during a pregnancy and almost 30% of early pregnancy may go unrecognized; the pathogenesis of pregnancy loss in this condition is still remains obscure. Compared with healthy women, the women with threatened miscarriage were found not only to have increased rate of antepartum haemorrhage, prelabour rupture of the membranes, preterm delivery, and intrauterine growth restriction, but also suffer from significant psychological impairment including considerable anxiety and stress, depression, sleep disturbances, anger, and marital disturbances.
To date, therapies have limited effectiveness in treating threatened miscarriage and are empirical. Bed rest does not prevent pregnancy loss. Acetaminophen may have some effects on relieving pain only. The most commonly used prescription medication was human chorionic gonadotropin (hCG), maintaining the luteotrophic effects to support continued secretion of estrogen and progesterone, but it's beneficial effects still cannot be verified. Progesterone is another most commonly used standard medication, maintaining the endometrial proliferation and preventing poor decidualization. A number of recent studies in women with threatened miscarriage shown a reduction in pregnancy loss with progesterone treatment. But progestogens are a group of hormones, including both the natural female sex hormone progesterone and the synthetic forms. Micronized progesterone is a kind of progesterone; it is structurally and pharmacologically very similar to natural progesterone and has good oral bioavailability. It is especially suitable for women with threatened miscarriage as it does not have androgenic or oestrogenic effects on the foetus. A recent review of maternal use of micronized progesterone during pregnancy also found no evidence for an increased risk of congenital malformations. However it may only be suitable to treat women with threatened miscarriage who have low progesterone levels due to corpus luteum deficiency at the first trimester of pregnancy. There is no evidence to show the beneficial effects of progesterone to treat threatened miscarriage due to others factors. At the same time, progesterone treatment is also expensive. New or adjuvant treatments that are suitable, readily accessible, affordable, and safe are needed to treat women with threatened miscarriage.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NSTW + OP | Experimental | NSTW one pack twice daily until 12 weeks of gestations (max 84 days); OP 100 mg thrice daily until 12 weeks of gestations (max 84 days). |
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| NSTW + OP placebo | Experimental | NSTW one pack twice daily until 12 weeks of gestations (max 84 days); OP Placebo 100 mg thrice daily until 12 weeks of gestations (max 84 days). |
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| NSTW Placebo + OP | Experimental | NSTW Placebo one pack twice daily until 12 weeks of gestations (max 84 days); OP 100 mg thrice daily until 12 weeks of gestations (max 84 days). |
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| NSTW Placebo + OP Placebo | Placebo Comparator | NSTW Placebo one pack twice daily until 12 weeks of gestations (max 84 days); OP Placebo 100 mg thrice daily until 12 weeks of gestations (max 84 days). |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Chinese Herbal Medicine (New "Shoutai Wan") plus Oral Progesterone | Drug | Chinese Herbal Medicine (New "Shoutai Wan", one pack twice daily) + Oral Progesterone (100 mg thrice daily) |
| Measure | Description | Time Frame |
|---|---|---|
| Live birth | Rate of live birth at or beyond 20 completed weeks' gestation | At or beyond 20 completed weeks' gestation |
| Measure | Description | Time Frame |
|---|---|---|
| Pregnancy outcome: Ongoing pregnancy | Rate of ongoing pregnancy (beyond 12 weeks' gestation) | Beyond 12 weeks' gestation |
| Pregnancy outcome: Miscarriage during the first trimester | Rate of miscarriage during the first trimester (at or before 12 weeks' gestation) |
| Measure | Description | Time Frame |
|---|---|---|
| Safety outcomes: Serious adverse events - Acute kidney injury (AKI) | Rate of acute kidney injury (AKI) | At any time during treatment (up to 2 months) and follow-up period (up to 1 year) |
| Safety outcomes: Serious adverse events - Drug induced liver injury (DILI) |
Inclusion criteria:
Exclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Xiao-Ke Wu, Ph.D | First Affiliated Hospital of Heilongjiang Chinese Medicine University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The First Affiliated Hospital of Anhui University of Chinese Medicine | Hefei | Anhui | China | |||
| Guangdong Provincial Hospital of Chinese Medicine |
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| Chinese Herbal Medicine (New "Shoutai Wan") plus Oral Progesterone Placebo | Drug | Chinese Herbal Medicine (New "Shoutai Wan", one pack twice daily) + Oral Progesterone Placebo (100 mg thrice daily) |
|
| Chinese Herbal Medicine Placebo (New "Shoutai Wan" placebo) plus Oral Progesterone | Drug | Chinese Herbal Medicine Placebo (New "Shoutai Wan" placebo, one pack twice daily) + Oral Progesterone (100 mg thrice daily) |
|
| Chinese Herbal Medicine Placebo (New "Shoutai Wan" placebo) plus Oral Progesterone Placebo | Drug | Chinese Herbal Medicine Placebo (New "Shoutai Wan" placebo, one pack twice daily) + Oral Progesterone Placebo (100 mg thrice daily) |
|
| During the first trimester (at or before 12 weeks' gestation) |
| Pregnancy outcome: Miscarriage during second and third trimesters | Rate of miscarriage during second and third trimesters (beyond 12 weeks' gestation until 20 weeks) | During second and third trimesters (beyond 12 weeks' gestation until 20 weeks) |
| Pregnancy outcome: Termination | Rate of termination at any time during treatment and follow-up period | At any time during treatment (up to 2 months) and follow-up period (up to 1 year) |
| Pregnancy outcome: Stillbirth | Rate of stillbirth (at or beyond 20 weeks' gestation) | At or beyond 20 weeks' gestation |
| Pregnancy outcome: Induced abortion | Rate of induced abortion at any time during treatment and follow-up for any reasons | At any time during treatment (up to 2 months) and follow-up period (up to 1 year) |
| Pregnancy outcome: Gestational age at delivery | Gestational age at delivery (weeks and days) | Up to 1 day after delivery |
| Pregnancy outcome: Preterm birth | Rate of preterm birth (birth beyond 28 week and before 37 completed weeks' gestation (up to and including 36 weeks and 6 days of gestation)) | Birth before 37 completed weeks' gestation (up to and including 36 weeks and 6 days of gestation) |
| Pregnancy outcome: Extreme preterm birth | Rate of extreme preterm birth (birth beyond 20 weeks and before 28 completed weeks' gestation (up to and including 27 weeks and 6 days of gestation)) | Birth beyond 20 weeks and before 28 completed weeks' gestation (up to and including 27 weeks and 6 days of gestation) |
| Pregnancy outcome: Full-term birth | Rate of full-term birth (at or beyond 37 weeks' gestation, and before 42 weeks' gestation) | At or beyond 37 weeks' gestation, and before 42 weeks' gestation |
| Pregnancy outcome: Post-term birth | Rate of post-term birth (at or beyond 42 weeks' gestation) | At or beyond 42 weeks' gestation |
| Neonatal outcome: Birth weight | Birth weight of neonatal (adjusted for gestational age and sex by Chinese standards) | When neonatal is born |
| Neonatal outcome: Small for gestational age | Rate of small for gestational age when neonatal is born | When neonatal is born |
| Neonatal outcome: Large for gestational age | Rate of large for gestational age when neonatal is born | When neonatal is born |
| Neonatal outcome: Congenital malformation | Rate of congenital malformation | At any time during treatment (up to 2 months) and follow-up period (up to 1 year) |
| Other outcome: Mean score change in TCM Symptom Questionnaire | Mean score change in TCM Symptom Questionnaire from baseline to the end of intervention. The questionnaire covers many dimensions including symptoms (amount of vaginal bleeding, severity of abdominal pain and other general symptoms), emotional factors and so on. The minimum and maximum value are depend on the symptoms of the patient respectively. | From date of randomization until the date of end of treatment, assessed up to 2 months |
| Other outcome: Mean score change in 12-Item Short-Form Health Survey | Mean score change in 12-Item Short-Form Health Survey from baseline to the end of intervention. The minimum value is 0 and the maximum value is 100, and higher scores mean a better outcome. | From date of randomization until the date of end of treatment, assessed up to 2 months |
| Other outcome: Mean score change in Self-Rating Anxiety Scale | Mean score change in Self-Rating Anxiety Scale from baseline to the end of intervention. The minimum value is 20 and the maximum value is 80, and lower scores mean a better outcome. | From date of randomization until the date of end of treatment, assessed up to 2 months |
Rate of drug induced liver injury (DILI) |
| At any time during treatment (up to 2 months) and follow-up period (up to 1 year) |
| Safety outcomes: Serious adverse events - Hospitalization | Rate of hospitalization (for threatened abortion in second and third trimester of pregnancy, hyperemesis gravidarum, aggravation-vaginal bleeding, cervical polypectomy, fall injuries and other reasons) | At any time during treatment (up to 2 months) and follow-up period (up to 1 year) |
| Safety outcomes: Adverse events - Nausea and vomiting | Rate of nausea and vomiting. | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Dizziness | Rate of Dizziness. | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Aadverse events - Fetal and neonatal complications | Rate of fetal and neonatal complications. Fetal complications including distress, and neonatal complications including early infection, NICU admission, pneumonia, hyperbilirubinemia. | From date of randomization until the date of end of pregnancy |
| Safety outcomes: Adverse events - Fatigue | Rate of Fatigue. | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Anorexia | Rate of Anorexia. | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Constipation | Rate of Constipation. | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Breast distention and pain | Rate of Breast distention and pain | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Upper respiratory tract infection | Rate of Upper respiratory tract infection. | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Abdominal pain | Rate of Abdominal pain | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Somnolence | Rate of Somnolence | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Insomnia | Rate of Insomnia | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Anemia | Rate of Anemia | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Diarrhea | Rate of Diarrhea | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Suspected acute kidney injury (AKI) | Rate of Suspected acute kidney injury (AKI) | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Adverse events - Suspected drug-induced liver injury (DILI). | Rate of Suspected drug-induced liver injury (DILI). | From date of randomization until the date of end of treatment, assessed up to 2 months. |
| Safety outcomes: Maternal complications - Pregnancy induced hypertension | Rate of Pregnancy induced hypertension | From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks. |
| Safety outcomes: Maternal complications - Pre-eclampsia | Rate of Pre-eclampsia | From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks. |
| Safety outcomes: Maternal complications - Gestational diabetes mellitus | Rate of Gestational diabetes mellitus | From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks. |
| Safety outcomes: Maternal complications - Placenta previa | Rate of Placenta previa | From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks. |
| Safety outcomes: Maternal complications - Pre-labour rupture of membranes | Rate of Pre-labour rupture of membranes | From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks. |
| Safety outcomes: Maternal complications - Postpartum haemorrhage | Rate of Postpartum haemorrhage | From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks. |
| Safety outcomes: Fetal complications - Fatal distress | Rate of Fatal distress | From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks. |
| Safety outcomes: Neonatal complications - Neonatal Early infection | Rate of Neonatal Early infection | From the date of delivery, assessed up to 6 weeks |
| Safety outcomes: Neonatal complications - Neonatal NICU admission | Rate of Neonatal NICU admission | From the date of delivery, assessed up to 6 weeks |
| Safety outcomes: Neonatal complications - Neonatal pneumonia | Rate of Neonatal pneumonia | From the date of delivery, assessed up to 6 weeks |
| Safety outcomes: Neonatal complications - Neonatal hyperbilirubinemia | Rate of Neonatal hyperbilirubinemia | From the date of delivery, assessed up to 6 weeks |
| Guangzhou |
| Guangdong |
| China |
| Peking University Shenzhen Hospital | Shenzhen | Guangdong | China |
| Da Qing Long Nan Hospital | Daqing | Heilongjiang | China |
| First Affiliated Hospital, Heilongjiang University of Chinese Medicine | Harbin | Heilongjiang | China |
| Luoyang Hospital of Traditional Chinese Medicine | Luoyang | Henan | China |
| The First Affiliated Hospital of Hunan University of Chinese Medicine | Changsha | Hunan | China |
| Changzhou Hospital of Traditional Chinese Medicine | Changzhou | Jiangsu | China |
| Suqian Maternity Hospital | Suqian | Jiangsu | China |
| The People's Hospital of Siyang | Suqian | Jiangsu | China |
| Xuzhou Central Hospital | Xuzhou | Jiangsu | China |
| Xuzhou Maternal and Child Health Hospital | Xuzhou | Jiangsu | China |
| Jiangxi Maternity and Child Health Hospital | Nanchang | Jiangxi | China |
| The Second Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine | Nanchang | Jiangxi | China |
| Dalian Maternal and Child Health Hospital | Dalian | Liaoning | China |
| Dalian women and children's medical group | Dalian | Liaoning | China |
| The First Affiliated Hospital of Liaoning University of Traditional Chinese Medicine | Shenyang | Liaoning | China |
| Ningxia Chinese Medicine Research Center | Yinchuan | Ningxia | China |
| Taian City Central Hospital | Tai’an | Shandong | China |
| Shanxi Traditional Chinese Medical Hospital | Taiyuan | Shanxi | China |
| Hangzhou Hospital of Traditional Chinese Medicine | Hangzhou | Zhejiang | China |
| Wenzhou TCM Hospital of Zhejiang Chinese Medical University | Wenzhou | Zhejiang | China |
| ID | Term |
|---|---|
| D000033 | Abortion, Threatened |
| ID | Term |
|---|---|
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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