ClinicalTrials.gov record
Terminated Phase 4 Interventional

Removal Versus Retention of Cerclage in Preterm Premature Rupture of Membranes (PPROM)

ClinicalTrials.gov ID: NCT00201656

Public ClinicalTrials.gov record NCT00201656. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 6:26 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Removal Versus Retention of Cervical Cerclage in Preterm Premature Rupture of Membranes-A Multicenter Randomized Clinical Trial

Study identification

NCT ID
NCT00201656
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Obstetrix Medical Group
Industry
Enrollment
58 participants

Conditions and interventions

Interventions

  • Removal of Cerclage Procedure
  • Removal vs. Retention of Cervical Cerclage Procedure
  • Retention of Cerclage Procedure

Procedure

Eligibility (public fields only)

Age range
18 Years to 60 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2004
Primary completion
Oct 31, 2013
Completion
Mar 31, 2014
Last update posted
Dec 18, 2014

2004 – 2014

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
Desert Good Samaritan Hospital Mesa Arizona 85202
Banner Good Samaritan Hospital Phoenix Arizona 85006
Tucson Medical Center Tucson Arizona 85712
Saddleback Memorial Medical Center Laguna Hills California 92653
Long Beach Memorial Medical Center Long Beach California 90801-1428
University of Southern California-Irvine Medical Center Orange California 92868
Good Samaritan Hospital San Jose California 95124
Swedish Medical Center Denver Colorado 80110
Presbyterian/St Luke's Hospital Denver Colorado 80218
Rose Medical Center Denver Colorado 80220
Yale New-Haven Medical Center New Haven Connecticut 06504
University of Illinois at Chicago Chicago Illinois 60612
Lousiana State University Health Science Shreveport Louisiana 60612
Hutzel Women's Hospital Detroit Michigan 48201
Saint Luke's Hospital, Kansas City Kansas City Missouri 64111
Sunrise Medical Center Las Vegas Nevada 89109
University of Rochester Medical Center Rochester New York 14642
The University Hospital Cincinnati Ohio 45219
Sacred Heart Medical Center Eugene Oregon 97401
Erlanger Medical Center Chattanooga Tennessee 37403
Memorial Hermann Children's Hospital-Texas Center for Fetal Assessment Houston Texas 77030
Evergreen Hospital Kirkland Washington 98034
Swedish Medical Center Seattle Washington 98122-4307

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00201656, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 18, 2014 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00201656 live on ClinicalTrials.gov.

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