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Preterm birth (PTB) is associated with over one million infant deaths annually worldwide. The incidence of PTB in the United States is 11.5% with more than 500,000 deliveries occurring at less than 37 weeks gestation annually. The rate of PTB in the United States increased to 12.8% in 2006, and remains high compared to almost all other developed countries, despite the introduction of many public health and medical interventions designed to delay PTB. Weekly treatment with 17-alpha hydroxyprogesterone caproate beginning at 16-20 weeks gestation has been shown to significantly reduce the risk of PTB and is currently recommended for women who experienced spontaneous PTB in a prior pregnancy. However, a strategy for the prevention of spontaneous PTBs in which therapeutic intervention is restricted to women with a previous PTB is likely to have a small effect on the overall rate of prematurity since only about 10% of spontaneous PTBs arise in women with such a history. A major reduction in rates of mortality and morbidity in premature babies will only be achieved with increased precision in the identification of women at risk of spontaneous PTB and through the development of an effective prevention for this complication. Transvaginal ultrasound measurement of cervical length is a reliable screening test for prediction of PTB. Although treatment with vaginal progesterone is effective in decreasing PTB in women with a short cervix, over 30% of women still experience premature delivery and many women find daily administration of progesterone to be challenging. Preliminary studies have suggested that use of an intravaginal pessary may be effective in preventing PTB. If effective this approach would be particularly appealing because of the wide availability of pessaries, ease of use, and low cost. Unfortunately, existing studies are inadequate to confirm effectiveness; a well designed, properly powered, prospective randomized trial is warranted prior to widespread implementation in clinical practice. We propose such a trial to study the effectiveness of the pessary in decreasing the incidence of PTB in an inner city Philadelphia population.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Pessary | Experimental | Use of the Bioteque cup pessary. Pessary will be placed between 18 and 23 6/7 weeks gestation, and will be removed during the 37th week of pregnancy (or earlier, if indicated) |
|
| No pessary | No Intervention | No pessary will be used. Subjects will receive standard obstetrical management |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Bioteque cup pessary | Device |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Subjects Experiencing Preterm Birth | Birth before 37 weeks gestation was captured. | Before 37 weeks gestation (20 0/7 - 36 6/7 weeks) |
| Measure | Description | Time Frame |
|---|---|---|
| Average Birth Weight of Babies Born on Trial | The birth weights of babies born in the pessary group was compared to those born in the no pessary group | Time of delivery |
| Number of Participants That Experienced Spontaneous Preterm Births on Trial |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Lorraine Dugoff, MD | University of Pennsylvania | Principal Investigator |
| Vincenzo Berghella, MD | Thomas Jefferson University | Principal Investigator |
| Jack Ludmir, MD | University of Pennsylvania | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Geisinger Medical Center | Danville | Pennsylvania | 17822 | United States | ||
| Hospital of the University of Pennsylvania |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 36453699 | Derived | Abdel-Aleem H, Shaaban OM, Abdel-Aleem MA, Aboelfadle Mohamed A. Cervical pessary for preventing preterm birth in singleton pregnancies. Cochrane Database Syst Rev. 2022 Dec 1;12(12):CD014508. doi: 10.1002/14651858.CD014508. |
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| ID | Title | Description |
|---|---|---|
| FG000 | Pessary | Use of the Bioteque cup pessary. Pessary will be placed between 18 and 23 6/7 weeks gestation, and will be removed during the 37th week of pregnancy (or earlier, if indicated) Bioteque cup pessary |
| FG001 | No Pessary | No pessary will be used. Subjects will receive standard obstetrical management |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Pessary | Use of the Bioteque cup pessary. Pessary will be placed between 18 and 23 6/7 weeks gestation, and will be removed during the 37th week of pregnancy (or earlier, if indicated) Bioteque cup pessary |
| BG001 | No Pessary |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Customized | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Subjects Experiencing Preterm Birth | Birth before 37 weeks gestation was captured. | Posted | Count of Participants | Participants | Before 37 weeks gestation (20 0/7 - 36 6/7 weeks) |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Pessary | Use of the Bioteque cup pessary. Pessary will be placed between 18 and 23 6/7 weeks gestation, and will be removed during the 37th week of pregnancy (or earlier, if indicated) Bioteque cup pessary |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Bacterial Vaginosis | Pregnancy, puerperium and perinatal conditions | Non-systematic Assessment | BV was accessed in both groups |
Our main limitation was the small sample size due to the fact that the study was stopped before planned enrollment was completed. In order to reach significance, we would need for the next 60 subjects randomized to the pessary group.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Bridget Nolan | University of Pennsylvania | 2156623324 | bridget.nolan@uphs.upenn.edu |
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| ID | Term |
|---|---|
| D047928 | Premature Birth |
| ID | Term |
|---|---|
| D007752 | Obstetric Labor, Premature |
| D007744 | Obstetric Labor Complications |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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The number of spontaneous births that occurred in participants on trial before 37 weeks was captured.
| Before 37 weeks gestation |
| Number of Participants Experiencing Spontaneous Rupture of Membranes | Rupture of membranes before 34 weeks gestation was captured in each group. | Less than 34 weeks gestation |
| Number of Subjects Experiencing Neonatal Death | Number of participants who experienced neonatal deaths from birth to day 28 was captured for each group. | Between birth and 28 days of age |
| Number of Subjects Experiencing Chorioamnionitis | The AE of Chorioamnionitis was captured for each group. | Time of delivery |
| Philadelphia |
| Pennsylvania |
| 19104 |
| United States |
| Pennsylvania Hospital | Philadelphia | Pennsylvania | 19107 | United States |
| Thomas Jefferson University Hospital | Philadelphia | Pennsylvania | 19107 | United States |
No pessary will be used. Subjects will receive standard obstetrical management
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Count of Participants | Participants |
|
| Units | Counts |
|---|
| Participants |
|
|
| Secondary | Average Birth Weight of Babies Born on Trial | The birth weights of babies born in the pessary group was compared to those born in the no pessary group | Posted | Mean | Full Range | grams | Time of delivery |
|
|
|
| Secondary | Number of Participants That Experienced Spontaneous Preterm Births on Trial | The number of spontaneous births that occurred in participants on trial before 37 weeks was captured. | Posted | Count of Participants | Participants | Before 37 weeks gestation |
|
|
|
| Secondary | Number of Participants Experiencing Spontaneous Rupture of Membranes | Rupture of membranes before 34 weeks gestation was captured in each group. | Posted | Count of Participants | Participants | Less than 34 weeks gestation |
|
|
|
| Secondary | Number of Subjects Experiencing Neonatal Death | Number of participants who experienced neonatal deaths from birth to day 28 was captured for each group. | Posted | Count of Participants | Participants | Between birth and 28 days of age |
|
|
|
| Secondary | Number of Subjects Experiencing Chorioamnionitis | The AE of Chorioamnionitis was captured for each group. | Posted | Count of Participants | Participants | Time of delivery |
|
|
|
| 0 |
| 61 |
| 0 |
| 61 |
| 3 |
| 61 |
| EG001 | No Pessary | No pessary will be used. Subjects will receive standard obstetrical management | 0 | 61 | 0 | 61 | 6 | 61 |
|
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| D000091642 | Urogenital Diseases |