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| ID | Type | Description | Link |
|---|---|---|---|
| H-35933 | Other Identifier | Baylor College of Medicine |
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The hypothesis of the investigators' project is that comprehensive primary preterm birth prevention, inclusive of maternal oral health with xylitol chewing gum (the intervention), will reduce the rate of periodontal disease and caries, preterm birth prevalence, and neonatal mortality.
Significance and Impact: Adverse birth outcomes related to the length of gestation (preterm birth) are recognized as one of the most significant disorders in maternal-child health at a global scale. In the developed world, the preterm birth rate approximates 7%. In Malawi, the investigators have recently demonstrated that this rate more than triples to approximate 26.1%. Of the 4 million newborn deaths annually, nearly 1/3 (27%) are directly attributable to prematurity with another 36% secondary to related opportunistic infections (sepsis, pneumonia, gastrointestinal). 75% of the 4 million deaths occur within the first week of life, with the vast majority occurring in the first 48 hours. For those that do survive, there are persistent and lifelong risks due to stunted growth, chronic infection, retinopathy of prematurity, and bronchopulmonary dysplasia. The link between maternal oral health (periodontal disease in particular) and risk of preterm birth has been demonstrated across all populations (rural and urban, in both industrialized and developing regions) studied to date. However, in multiple randomized controlled trials treatment of active periodontal disease with scaling and planning during pregnancy has failed to demonstrate a significant benefit in preventing preterm birth.
Why would maternal oral health impact preterm birth? In rodents, subcutaneous inoculations with periodontal pathogens cause dose-dependent decreases in pup weights, and elicit inflammatory responses that can trigger preterm birth when present in amniotic fluid. Periodontitis (defined as a destructive inflammation of the periodontium) has a prevalence of 30% or greater in women of child bearing age. By definition, it involves microbial infiltration of the periodontium, which stimulates a chronic inflammatory response, recurrent bacteremia, and the production of cytokines and prostaglandins which trigger risk of preterm birth. It is the same production of prostaglandins which are felt to mediate the risk of preterm birth. So if the investigators know that there is biologic evidence that periodontitis is related to preterm birth, but treating active periodontitis does not reduce these morbidities, is it possible that preventing periodontitis might prevent preterm birth and low birth weight? If so, what are the least expensive efficacious preventative measures? The investigators' overarching hypothesis is that comprehensive primary preterm birth prevention, inclusive of maternal oral health with xylitol chewing gum (the intervention), will reduce the rate of periodontal disease and caries, preterm birth prevalence, and neonatal mortality.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control | No Intervention | Cluster of sites not receiving xylitol gum. This is a cluster randomized trial, whereby 4 sites will not receive the intervention of xylitol gum in the prepregnancy and early pregnancy interval. | |
| Xylitol | Experimental | Cluster of sites receiving xylitol gum. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Xylitol gum | Dietary Supplement | This is a cluster randomized trial, whereby 4 sites will receive the intervention of xylitol gum in the prepregnancy and early pregnancy interval. |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of Preterm Birth | This is a co-primary outcome: Measure rate of preterm birth <37 weeks gestation, as defined by best obstetrical estimate based upon last menstrual period correlated with fundal height at entry to prenatal care or ultrasound, when available; all sites have access to referral for ultrasound. | Conception to date of delivery, <37 weeks gestation |
| Number of Infants <2500 Grams | This is a co-primary outcome: Measured weight at delivery to determine the rate of <2500 gram infants. | Date of delivery to 1 week postnatal |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Infants With Adverse Neonatal Composite Morbidity and Mortality | Additive or singular composite neonatal morbidity up to 28 days of age. Composite neonatal morbidity and mortality outcomes are defined as: neonatal death, miscarriage <28 weeks, stillbirth (fresh or macerated), neonatal sepsis, neonatal respiratory distress, neonatal seizures, feeding problems, fever, hypothermia, Apgar score <7 at 5 minutes after birth, referral to other hospital or neonatal intensive care unit (NICU) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Kjersti Aagaard, M.D. | Baylor College of Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Baylor College of Medicine | Houston | Texas | 77030 | United States |
All patients who were eligible and consented for the study were enrolled and designated into either a control or intervention group based on this cluster-randomized design and the site of enrollment where the participant initially presented.
Recruitment through outpatient prenatal clinics
| ID | Title | Description |
|---|---|---|
| FG000 | Control | Cluster of sites not receiving xylitol gum. This is a cluster randomized trial, whereby 4 sites will not receive the intervention of xylitol gum in the prepregnancy and early pregnancy interval. |
| FG001 | Xylitol | Cluster of sites receiving xylitol gum. Xylitol gum: This is a cluster randomized trial, whereby 4 sites will receive the intervention of xylitol gum in the prepregnancy and early pregnancy interval. |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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Includes 10069 total individuals who were eligible and enrolled in the PPaX trial.
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| ID | Title | Description |
|---|---|---|
| BG000 | Control | Cluster of sites not receiving xylitol gum. This is a cluster randomized trial, whereby 4 sites will not receive the intervention of xylitol gum in the prepregnancy and early pregnancy interval. |
| BG001 | Xylitol |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| 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 | Rate of Preterm Birth | This is a co-primary outcome: Measure rate of preterm birth <37 weeks gestation, as defined by best obstetrical estimate based upon last menstrual period correlated with fundal height at entry to prenatal care or ultrasound, when available; all sites have access to referral for ultrasound. | Posted | Count of Participants | Participants | Conception to date of delivery, <37 weeks gestation |
|
4 years; Data was collected from study enrollment in 2015 through 2019 during which study participants were enrolled and completed the study. An additional 2 year follow-up period occurred from 2019-2021 in which data was verified and cross-validated with local maternal delivery logbooks
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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 | Control | Cluster of sites not receiving xylitol gum. This is a cluster randomized trial, whereby 4 sites will not receive the intervention of xylitol gum in the prepregnancy and early pregnancy interval. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Death | Pregnancy, puerperium and perinatal conditions | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Kjersti Aagaard | Baylor College of Medicine, Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine | 7137988467 | aagaardt@bcm.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP_ICF | Yes | Yes | Yes | Study Protocol, Statistical Analysis Plan, and Informed Consent Form | Nov 1, 2021 | Mar 15, 2022 | Prot_SAP_ICF_000.pdf |
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| ID | Term |
|---|---|
| D047928 | Premature Birth |
| D010510 | Periodontal Diseases |
| D003731 | Dental Caries |
| ID | Term |
|---|---|
| D007752 | Obstetric Labor, Premature |
| D007744 | Obstetric Labor Complications |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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| Date of delivery to 28 days postnatal |
| Number of Participants With Periodontal Disease | We will measure the prevalence of periodontal disease among gravidae. We will use standardized World Health Organization (WHO) oral health forms and disease scoring. | During pregnancy, up to 2 dental visits performed during pregnancy (approximately 37-40 weeks if term) to evaluate dental outcomes |
| Number of Participants With Dental Caries | We will measure the prevalence of dental caries among gravidae. We will use standardized World Health Organization (WHO) oral health forms and disease scoring. | During pregnancy, up to 2 dental visits performed during pregnancy (approximately 37-40 weeks if term) to evaluate dental outcomes |
| Enrolled prepregnant without neonatal outcome data available |
|
Cluster of sites receiving xylitol gum.
Xylitol gum: This is a cluster randomized trial, whereby 4 sites will receive the intervention of xylitol gum in the prepregnancy and early pregnancy interval.
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race/Ethnicity, Customized | Count of Participants | Participants |
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| Region of Enrollment | Number | participants |
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| Units | Counts |
|---|---|
| Participants |
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|
|
| Primary | Number of Infants <2500 Grams | This is a co-primary outcome: Measured weight at delivery to determine the rate of <2500 gram infants. | There were 5260 of the 5520 subjects in the control group after removing 42 with an interrupted pregnancy, 20 prepregnant without information on neonatal outcomes, 137 lost to follow up, and 61 with only neonatal gestational age information. There were 4305 of 4349 consented for enrollment in the xylitol intervention group, after removing 89 with an interrupted pregnancy, 5 prepregnant without neonatal outcomes data, 106 lost to follow up and 45 with only neonatal gestational age data. | Posted | Count of Participants | Participants | Date of delivery to 1 week postnatal |
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| Secondary | Number of Infants With Adverse Neonatal Composite Morbidity and Mortality | Additive or singular composite neonatal morbidity up to 28 days of age. Composite neonatal morbidity and mortality outcomes are defined as: neonatal death, miscarriage <28 weeks, stillbirth (fresh or macerated), neonatal sepsis, neonatal respiratory distress, neonatal seizures, feeding problems, fever, hypothermia, Apgar score <7 at 5 minutes after birth, referral to other hospital or neonatal intensive care unit (NICU) | Posted | Count of Participants | Participants | Date of delivery to 28 days postnatal |
|
|
|
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| Secondary | Number of Participants With Periodontal Disease | We will measure the prevalence of periodontal disease among gravidae. We will use standardized World Health Organization (WHO) oral health forms and disease scoring. | There were 461 subjects in the control group who completed at least 2 dental visits. There were 490 subjects in the intervention, xylitol group who completed at least 2 dental visits. | Posted | Count of Participants | Participants | During pregnancy, up to 2 dental visits performed during pregnancy (approximately 37-40 weeks if term) to evaluate dental outcomes |
|
|
|
|
| Secondary | Number of Participants With Dental Caries | We will measure the prevalence of dental caries among gravidae. We will use standardized World Health Organization (WHO) oral health forms and disease scoring. | There were 461 subjects in the control group who completed at least 2 dental visits. There were 490 subjects in the intervention, xylitol group who completed at least 2 dental visits. | Posted | Count of Participants | Participants | During pregnancy, up to 2 dental visits performed during pregnancy (approximately 37-40 weeks if term) to evaluate dental outcomes |
|
|
|
|
| 2 |
| 5,520 |
| 2 |
| 5,520 |
| 0 |
| 5,520 |
| EG001 | Xylitol | Cluster of sites receiving xylitol gum. Xylitol gum: This is a cluster randomized trial, whereby 4 sites will receive the intervention of xylitol gum in the prepregnancy and early pregnancy interval. | 0 | 4,549 | 0 | 4,549 | 0 | 4,549 |
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| D000091642 | Urogenital Diseases |
| D009059 | Mouth Diseases |
| D009057 | Stomatognathic Diseases |
| D017001 | Tooth Demineralization |
| D014076 | Tooth Diseases |