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N/A N=122 Randomized Prevention

Prevention of Preterm Birth With a Pessary in Singleton Gestations

Preterm Birth · Short Cervix

Enrolled (actual)
122
Serious AEs
0.0%
Results posted
May 2018
Primary outcome: Primary: Number of Subjects Experiencing Preterm Birth — 26; 23 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Bioteque cup pessary (Device)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
University of Pennsylvania
Primary completion
Sep 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Subjects Experiencing Preterm Birth
26; 23
SECONDARY
Average Birth Weight of Babies Born on Trial
2788; 2843
SECONDARY
Number of Participants That Experienced Spontaneous Preterm Births on Trial
23; 19
SECONDARY
Number of Participants Experiencing Spontaneous Rupture of Membranes
18; 10
SECONDARY
Number of Subjects Experiencing Neonatal Death
3; 6
SECONDARY
Number of Subjects Experiencing Chorioamnionitis
7; 4

Summary

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.

Eligibility Criteria

Inclusion Criteria

  • 18-50 years of age
  • Singleton pregnancy (limits the participants to female gender)
  • Short cervical length (less than or equal to 25 mm) on second trimester ultrasound at 18-23 6/7 weeks gestation

Exclusion Criteria

  • Multiple gestation
  • Prior spontaneous preterm birth 16-36 6/7 weeks
  • Ruptured membranes
  • Lethal fetal structural anomaly
  • Fetal chromosomal abnormality
  • Cerclage in place (or planned placement)
  • Vaginal bleeding
  • Suspicion of chorioamnionitis
  • Ballooning of membranes outside the cervix into the vagina or CL = 0 mm on transvaginal ultrasound
  • Painful regular uterine contractions
  • Placenta previa
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02056652). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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