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NCT00059683 · ClinicalTrials.gov registry record · NA

Ultrasound-indicated Cerclage to Prevent Premature Birth in High-risk Women

A NA study, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

Completed
Registry status
NA
Development phase
300
Enrollment target

NCT00059683 is a NA study that has completed, run by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). The registered enrollment target is 300 participants.

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The verdict

NCT00059683, a NA study, has completed, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

COMPLETED
Registry status
NA
Development phase
300 participants
Enrollment target

Study Summary

Pregnant women who have a shortened cervix and have previously had a premature baby are at increased risk for having another premature baby. This study will determine whether reinforcing the cervix with a surgical stitch can reduce the chance of a premature birth.

Interventions

  • PROCEDURE cervical cerclage

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2003-01
Est. Completion 2009-10
Phase NA

What the Registry Record Tells You About NCT00059683

The ClinicalTrials.gov registry entry for NCT00059683 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), which has 305 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which cervical cerclage is the first listed.

NCT00059683 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00059683 about?

NCT00059683 is a clinical study titled "Ultrasound-indicated Cerclage to Prevent Premature Birth in High-risk Women". Pregnant women who have a shortened cervix and have previously had a premature baby are at increased risk for having another premature baby. This study will determine whether reinforcing the cervix with a surgical stitch can reduce the chance of a premature birth.

What is the current status of trial NCT00059683?

This trial is currently completed. It is a NA study. The enrollment target is 300 participants. The study started on 2003-01. Estimated completion is 2009-10.

What interventions are being tested in trial NCT00059683?

The interventions under investigation include: cervical cerclage (PROCEDURE).

Who is sponsoring clinical trial NCT00059683?

This trial is sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), which has 305 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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