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Prevention of Preterm Birth With a Pessary in Twin Gestations (PoPPT)

Primary Purpose

Premature 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 Premature Birth focused on measuring Premature birth, Premature delivery, Short cervix, Pessary

Eligibility Criteria

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

Inclusion Criteria:

  • 18-50 years of age
  • Twin pregnancy (limits the participants to female gender)
  • Short cervical length (less than or equal to 30 mm) on second trimester ultrasound at 18-27 6/7 weeks gestation

Exclusion Criteria:

  • Singleton or higher order than twins multiple gestation
  • Monoamniotic twins
  • Twin twin transfusion syndrome
  • 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
  • Painful regular uterine contractions
  • Labor
  • Placenta previa

Sites / Locations

  • 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 27 6/7 weeks gestation, and will be removed during the 36th week of pregnancy (or earlier if indicated)

No pessary will be used. Subjects will receive standard obstetrical management

Outcomes

Primary Outcome Measures

Number of Participants With Preterm Delivery

Secondary Outcome Measures

Average Birth Weight of Babies in Each Group
The birth weight of babies is the pessary group and no pessary group were recorded and analyzed for comparison.
Spontaneous Preterm Birth Rates
Number of Participants That Experienced Neonatal Death
Number of participants that experienced neonatal deaths that occurred in each group following birth was recorded and analyzed.
Number of Subjects Experiencing Chorioamnionitis
Chorioamnionitis was recorded and analyzed for participants in 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
NCT02056639
Brief Title
Prevention of Preterm Birth With a Pessary in Twin Gestations
Acronym
PoPPT
Official Title
Prevention of Preterm Birth With a Pessary in Twin 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
August 2016 (Actual)
Study Completion Date
October 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 a major health problem and contributes to more than 50% of the overall perinatal mortality. Twins are at increased risk for PTB. The number of twins births has risen substantially due to the increased use of assisted reproductive technology. The rate of twin births in the United States rose from 18.9 to 32.2 per 100 live births between 1980 and 2004. The increased rate of PTB in twins is associated with increased morbidity and mortality rates. Almost one in four very low birth-weight infants (below 1500 g) born in the United States are twins, as are one in six infants who die in the first month of life. Cervical shortening is a risk factor for PTB. Transvaginal ultrasound measurement of cervical length is a reliable screening test for prediction of PTB. There is currently no effective treatment to decrease the incidence of PTB in women with twin gestations, but there is some evidence that the use of a cervical pessary in women with a short cervix has promise. 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
Premature Birth, Short Cervix
Keywords
Premature birth, Premature 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
46 (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 27 6/7 weeks gestation, and will be removed during the 36th 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 Participants With Preterm Delivery
Time Frame
Less than 34 weeks gestation
Secondary Outcome Measure Information:
Title
Average Birth Weight of Babies in Each Group
Description
The birth weight of babies is the pessary group and no pessary group were recorded and analyzed for comparison.
Time Frame
Time of delivery
Title
Spontaneous Preterm Birth Rates
Time Frame
Less than 37 weeks gestation
Title
Number of Participants That Experienced Neonatal Death
Description
Number of participants that experienced neonatal deaths that occurred in each group following birth was recorded and analyzed.
Time Frame
Between birth and 28 days of age
Title
Number of Subjects Experiencing Chorioamnionitis
Description
Chorioamnionitis was recorded and analyzed for participants in 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 Twin pregnancy (limits the participants to female gender) Short cervical length (less than or equal to 30 mm) on second trimester ultrasound at 18-27 6/7 weeks gestation Exclusion Criteria: Singleton or higher order than twins multiple gestation Monoamniotic twins Twin twin transfusion syndrome 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 Painful regular uterine contractions Labor 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
Organizational Affiliation
Thomas Jefferson University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jack Ludmir
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
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 Twin Gestations

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