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Progesterone for Prevention of Preterm Birth in Women With Short Cervix: Randomized Controlled Trial

Primary Purpose

Preterm Birth, Pregnancy Trimester, Second

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Micronised progesterone (Utrogestan)
Sponsored by
King's College Hospital NHS Trust
About
Eligibility
Locations
Outcomes
Full info

About this trial

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

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • All women with singleton or twin pregnancies attending for routine ultrasound examination at 20-25 weeks of gestation with a short cervical length (<15 mm).

Exclusion Criteria:

  • Women with major fetal abnormalities,
  • Painful regular uterine contractions, or history of ruptured membranes or cervical cerclage in-situ were excluded from screening.

Sites / Locations

  • Hospital do Servidor Publico Estadual-FMO
  • Hospital Clinico Universidad de Chile
  • University Hospital
  • Darent Valley Hospital
  • University Hospital of Lewisham
  • Queen Elizabeth Hospital, NHS Trust Woolwich
  • King's College Hospital NHS Foumdation Trust
  • Southend University Hospital, Essex

Outcomes

Primary Outcome Measures

Spontaneous delivery before 34 completed weeks (238 days) of gestation.

Secondary Outcome Measures

Birth weight, fetal or neonatal death, major adverse outcome before discharge from hospital and need for neonatal special care (admission to special care baby unit, phototherapy, treatment of proven or suspected sepsis, or blood transfusion).

Full Information

First Posted
January 15, 2007
Last Updated
January 16, 2007
Sponsor
King's College Hospital NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT00422526
Brief Title
Progesterone for Prevention of Preterm Birth in Women With Short Cervix: Randomized Controlled Trial
Official Title
Randomised Study to Examine the Effectiveness of Progesterone in Preventing Severe Preterm Delivery
Study Type
Interventional

2. Study Status

Record Verification Date
January 2007
Overall Recruitment Status
Completed
Study Start Date
September 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
King's College Hospital NHS Trust

4. Oversight

5. Study Description

Brief Summary
The aim of our study is to evaluate the effect of use of prophylactic vaginal progesterone on the incidence of severe preterm delivery, defined as delivery before 33+6 weeks in women with a short cervical length of 15mm.
Detailed Description
BACKGROUND The results of randomized studies have shown that the prophylactic use of progesterone in women who previously delivered prematurely reduces the risk of recurrence. Asymptomatic women found to have a short cervix (< 15 mm) at mid-gestation are at greatly increased risk for spontaneous early preterm delivery and it is uncertain whether in such women the risk is reduced by progesterone. METHODS Cervical length was measured by transvaginal sonography at 22 (range 20-25) weeks in 24,620 pregnant women attending for routine antenatal care. The cervix was 15 mm or less in 413 (1.7%), and 250 (60.5%) of these women participated in a randomized study of vaginal progesterone (200 mg per night) vs identical-looking placebo, between 24 and 34 weeks. Primary outcome was the frequency of spontaneous delivery before 34 weeks (238 days) of pregnancy. Analysis was performed according to the intention-to-treat principle.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Birth, Pregnancy Trimester, Second
Keywords
Preterm delivery, short cervix, progesterone

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
Double
Allocation
Randomized
Enrollment
250 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Micronised progesterone (Utrogestan)
Primary Outcome Measure Information:
Title
Spontaneous delivery before 34 completed weeks (238 days) of gestation.
Secondary Outcome Measure Information:
Title
Birth weight, fetal or neonatal death, major adverse outcome before discharge from hospital and need for neonatal special care (admission to special care baby unit, phototherapy, treatment of proven or suspected sepsis, or blood transfusion).

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All women with singleton or twin pregnancies attending for routine ultrasound examination at 20-25 weeks of gestation with a short cervical length (<15 mm). Exclusion Criteria: Women with major fetal abnormalities, Painful regular uterine contractions, or history of ruptured membranes or cervical cerclage in-situ were excluded from screening.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kypros H Nicolaides, MD, PhD
Organizational Affiliation
King's College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital do Servidor Publico Estadual-FMO
City
Sao Paulo
Country
Brazil
Facility Name
Hospital Clinico Universidad de Chile
City
Santiago
Country
Chile
Facility Name
University Hospital
City
Larissa
Country
Greece
Facility Name
Darent Valley Hospital
City
Kent
Country
United Kingdom
Facility Name
University Hospital of Lewisham
City
London
ZIP/Postal Code
SE13 6LH
Country
United Kingdom
Facility Name
Queen Elizabeth Hospital, NHS Trust Woolwich
City
London
ZIP/Postal Code
SE18 4QH
Country
United Kingdom
Facility Name
King's College Hospital NHS Foumdation Trust
City
London
ZIP/Postal Code
SE5 9RS
Country
United Kingdom
Facility Name
Southend University Hospital, Essex
City
London
ZIP/Postal Code
SS0 0RY
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
17671254
Citation
Fonseca EB, Celik E, Parra M, Singh M, Nicolaides KH; Fetal Medicine Foundation Second Trimester Screening Group. Progesterone and the risk of preterm birth among women with a short cervix. N Engl J Med. 2007 Aug 2;357(5):462-9. doi: 10.1056/NEJMoa067815.
Results Reference
derived

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Progesterone for Prevention of Preterm Birth in Women With Short Cervix: Randomized Controlled Trial

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