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Does Progesterone Prevent Very Preterm Delivery in Twin Pregnancies?

Primary Purpose

Preterm Delivery

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Progesterone
Placebo
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Preterm Delivery focused on measuring Preterm delivery, Prevention, Twins, Progesterone

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Twin pregnancy Informed consent 18-23 weeks' gestation Participants must be fluent in the language spoken in the respective centres Exclusion Criteria: Age < 18 years Known allergy to progesterone or peanuts Active thromboembolic disorders or a history of hormone-associated thromboembolic disorders Rupture of membranes at the time of inclusion Monoamniotic twins Pregnancies treated for or with signs of twin-to-twin transfusion syndrome at inclusion Multiple pregnancies reduced to twin pregnancies Known significant structural or chromosomal fetal abnormality Chorionicity not assessed before 15 weeks Known or suspected malignancy in genitals or breasts Known liver disease

Sites / Locations

  • Graz University Hospital
  • Innsbruck University Hospital
  • Klagenfurt Hospital
  • Vienna University Hospital
  • Aalborg Hospital
  • Skejby Hospital
  • Rigshospitalet
  • Glostrup Hospital
  • Gentofte Hospital
  • Herlev Hospital
  • Hilleroed Hospital
  • Holbaek Hospital
  • Hvidovre Hospital
  • Odense University Hospital
  • Roskilde Hospital
  • Soenderborg Hospital
  • Viborg Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Progesterone

Arm Description

Outcomes

Primary Outcome Measures

The incidence of delivery < 34 weeks, in the study group versus the control group

Secondary Outcome Measures

Physical and neurological development of the children at 6 and 18 months
The relationship between cervical length and prophylactic progesterone treatment
Determination of proteomics and RNA in preterm delivery and term delivery and an evaluation of the effect of progesterone on proteomics and RNA
Assessment of the potential anti-inflammatory effect of progesterone by cytokine-measurements
Assessment of the effect of progesterone on CRH-levels in twin pregnancies

Full Information

First Posted
May 24, 2006
Last Updated
July 22, 2011
Sponsor
Rigshospitalet, Denmark
Collaborators
The Danish Medical Research Council, The Danish Medical Society in Copenhagen, AP Moeller Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00329914
Brief Title
Does Progesterone Prevent Very Preterm Delivery in Twin Pregnancies?
Official Title
Effectiveness of Vaginally Administered Progesterone to Prevent Preterm Delivery in Twin Pregnancies - A Multicentre Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
June 2006 (undefined)
Primary Completion Date
February 2009 (Actual)
Study Completion Date
September 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Rigshospitalet, Denmark
Collaborators
The Danish Medical Research Council, The Danish Medical Society in Copenhagen, AP Moeller Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to determine whether a daily dose of 200 mg progesterone administered vaginally from 20-23 to 34 weeks' gestation will reduce the rate of preterm delivery amongst twin pregnancies.
Detailed Description
Multiple gestations account for 2% of all pregnancies, but cause more than 10% of the cases of preterm delivery. Due to increasing maternal age and use of assisted reproduction the number of multiple gestations is larger than ever. If markers of preterm delivery can be identified and means of preventing preterm delivery are found, it will be possible to reduce the number of children admitted to hospital because of prematurity. Recently, two larger randomised studies investigated the effect of progesterone in singleton pregnancies of women who had previously delivered preterm. They both found a significant reduction in the preterm delivery rate in the progesterone group compared to a placebo group. The study will be performed as a randomized, double-blind placebo controlled study of twin pregnancies in Denmark and Austria. The women will be randomised in a 1:1 ratio to two groups (progesterone versus placebo). Randomisation will be stratified per centre and according to chorionicity, as the risk of preterm delivery is doubled in monochorionic twins compared to dichorionic twins.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Delivery
Keywords
Preterm delivery, Prevention, Twins, Progesterone

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
677 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Progesterone
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Progesterone
Other Intervention Name(s)
Utrogestan
Intervention Description
Vaginal pessaries, 200 mg/day
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo pessaries containing peanut oil
Primary Outcome Measure Information:
Title
The incidence of delivery < 34 weeks, in the study group versus the control group
Time Frame
Participants will be followed until 3 weeks after delivery
Secondary Outcome Measure Information:
Title
Physical and neurological development of the children at 6 and 18 months
Time Frame
2 years after delivery
Title
The relationship between cervical length and prophylactic progesterone treatment
Time Frame
Participants will be followed until 3 weeks after delivery
Title
Determination of proteomics and RNA in preterm delivery and term delivery and an evaluation of the effect of progesterone on proteomics and RNA
Time Frame
Participants will be followed until 3 weeks after delivery
Title
Assessment of the potential anti-inflammatory effect of progesterone by cytokine-measurements
Time Frame
Participants will be followed until 3 weeks after delivery
Title
Assessment of the effect of progesterone on CRH-levels in twin pregnancies
Time Frame
Participants will be followed until 3 weeks after delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Twin pregnancy Informed consent 18-23 weeks' gestation Participants must be fluent in the language spoken in the respective centres Exclusion Criteria: Age < 18 years Known allergy to progesterone or peanuts Active thromboembolic disorders or a history of hormone-associated thromboembolic disorders Rupture of membranes at the time of inclusion Monoamniotic twins Pregnancies treated for or with signs of twin-to-twin transfusion syndrome at inclusion Multiple pregnancies reduced to twin pregnancies Known significant structural or chromosomal fetal abnormality Chorionicity not assessed before 15 weeks Known or suspected malignancy in genitals or breasts Known liver disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Line Rode, MD
Organizational Affiliation
Ultrasound Clinic 4002, Rigshospitalet
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ann Tabor, professor
Organizational Affiliation
Ultrasound Clinic 4002, Rigshospitalet
Official's Role
Study Director
Facility Information:
Facility Name
Graz University Hospital
City
Graz
ZIP/Postal Code
8036
Country
Austria
Facility Name
Innsbruck University Hospital
City
Innsbruck
ZIP/Postal Code
6020
Country
Austria
Facility Name
Klagenfurt Hospital
City
Klagenfurt
ZIP/Postal Code
9020
Country
Austria
Facility Name
Vienna University Hospital
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Facility Name
Aalborg Hospital
City
Aalborg
ZIP/Postal Code
9100
Country
Denmark
Facility Name
Skejby Hospital
City
Aarhus
ZIP/Postal Code
8200
Country
Denmark
Facility Name
Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Facility Name
Glostrup Hospital
City
Glostrup
ZIP/Postal Code
2600
Country
Denmark
Facility Name
Gentofte Hospital
City
Hellerup
ZIP/Postal Code
2900
Country
Denmark
Facility Name
Herlev Hospital
City
Herlev
ZIP/Postal Code
2730
Country
Denmark
Facility Name
Hilleroed Hospital
City
Hilleroed
ZIP/Postal Code
3400
Country
Denmark
Facility Name
Holbaek Hospital
City
Holbaek
ZIP/Postal Code
4300
Country
Denmark
Facility Name
Hvidovre Hospital
City
Hvidovre
ZIP/Postal Code
2650
Country
Denmark
Facility Name
Odense University Hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Facility Name
Roskilde Hospital
City
Roskilde
ZIP/Postal Code
4000
Country
Denmark
Facility Name
Soenderborg Hospital
City
Soenderborg
ZIP/Postal Code
6400
Country
Denmark
Facility Name
Viborg Hospital
City
Viborg
ZIP/Postal Code
8800
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
21739497
Citation
Rode L, Klein K, Nicolaides KH, Krampl-Bettelheim E, Tabor A; PREDICT Group. Prevention of preterm delivery in twin gestations (PREDICT): a multicenter, randomized, placebo-controlled trial on the effect of vaginal micronized progesterone. Ultrasound Obstet Gynecol. 2011 Sep;38(3):272-80. doi: 10.1002/uog.9093.
Results Reference
result
PubMed Identifier
21739499
Citation
Klein K, Rode L, Nicolaides KH, Krampl-Bettelheim E, Tabor A; PREDICT Group. Vaginal micronized progesterone and risk of preterm delivery in high-risk twin pregnancies: secondary analysis of a placebo-controlled randomized trial and meta-analysis. Ultrasound Obstet Gynecol. 2011 Sep;38(3):281-7. doi: 10.1002/uog.9092.
Results Reference
result
PubMed Identifier
22914392
Citation
Rode L, Klein K, Larsen H, Holmskov A, Andreasen KR, Uldbjerg N, Ramb J, Bodker B, Skibsted L, Sperling L, Hinterberger S, Krebs L, Zingenberg H, Weiss EC, Strobl I, Laursen L, Christensen JT, Skogstrand K, Hougaard DM, Krampl-Bettelheim E, Rosthoj S, Vogel I, Tabor A. Cytokines and the risk of preterm delivery in twin pregnancies. Obstet Gynecol. 2012 Jul;120(1):60-8. doi: 10.1097/AOG.0b013e31825bc3cd.
Results Reference
derived
Links:
URL
http://clinicaltrials.gov/ct2/show/NCT00329914
Description
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Does Progesterone Prevent Very Preterm Delivery in Twin Pregnancies?

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