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Prevention of Preterm Birth With a Pessary in Singleton Gestations (PoPPS)

Primary Purpose

Preterm Birth, Short Cervix

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bioteque cup pessary
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Preterm Birth focused on measuring Preterm birth, Preterm delivery, short cervix, pessary

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

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

Sites / Locations

  • Geisinger Medical Center
  • Hospital of the University of Pennsylvania
  • Pennsylvania Hospital
  • Thomas Jefferson University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Pessary

No pessary

Arm Description

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 will be used. Subjects will receive standard obstetrical management

Outcomes

Primary Outcome Measures

Number of Subjects Experiencing Preterm Birth
Birth before 37 weeks gestation was captured.

Secondary Outcome Measures

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
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.
Number of Participants Experiencing Spontaneous Rupture of Membranes
Rupture of membranes before 34 weeks gestation was captured in each group.
Number of Subjects Experiencing Neonatal Death
Number of participants who experienced neonatal deaths from birth to day 28 was captured for each group.
Number of Subjects Experiencing Chorioamnionitis
The AE of Chorioamnionitis was captured for each group.

Full Information

First Posted
February 4, 2014
Last Updated
April 27, 2018
Sponsor
University of Pennsylvania
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1. Study Identification

Unique Protocol Identification Number
NCT02056652
Brief Title
Prevention of Preterm Birth With a Pessary in Singleton Gestations
Acronym
PoPPS
Official Title
Prevention of Preterm Birth With a Pessary in Singleton Gestations
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
February 2014 (Actual)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Pennsylvania

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Birth, Short Cervix
Keywords
Preterm birth, Preterm delivery, short cervix, pessary

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
122 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pessary
Arm Type
Experimental
Arm Description
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)
Arm Title
No pessary
Arm Type
No Intervention
Arm Description
No pessary will be used. Subjects will receive standard obstetrical management
Intervention Type
Device
Intervention Name(s)
Bioteque cup pessary
Primary Outcome Measure Information:
Title
Number of Subjects Experiencing Preterm Birth
Description
Birth before 37 weeks gestation was captured.
Time Frame
Before 37 weeks gestation (20 0/7 - 36 6/7 weeks)
Secondary Outcome Measure Information:
Title
Average Birth Weight of Babies Born on Trial
Description
The birth weights of babies born in the pessary group was compared to those born in the no pessary group
Time Frame
Time of delivery
Title
Number of Participants That Experienced Spontaneous Preterm Births on Trial
Description
The number of spontaneous births that occurred in participants on trial before 37 weeks was captured.
Time Frame
Before 37 weeks gestation
Title
Number of Participants Experiencing Spontaneous Rupture of Membranes
Description
Rupture of membranes before 34 weeks gestation was captured in each group.
Time Frame
Less than 34 weeks gestation
Title
Number of Subjects Experiencing Neonatal Death
Description
Number of participants who experienced neonatal deaths from birth to day 28 was captured for each group.
Time Frame
Between birth and 28 days of age
Title
Number of Subjects Experiencing Chorioamnionitis
Description
The AE of Chorioamnionitis was captured for each group.
Time Frame
Time of delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lorraine Dugoff, MD
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Vincenzo Berghella, MD
Organizational Affiliation
Thomas Jefferson University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jack Ludmir, MD
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
Facility Name
Geisinger Medical Center
City
Danville
State/Province
Pennsylvania
ZIP/Postal Code
17822
Country
United States
Facility Name
Hospital of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Pennsylvania Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Thomas Jefferson University Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States

12. IPD Sharing Statement

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Prevention of Preterm Birth With a Pessary in Singleton Gestations

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