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NCT00371046 · ClinicalTrials.gov registry record · NA
Does Fetal Fibronectin and Ultrasound Cervical Length Help in the Evaluation of Women With Suspected Preterm Labor?
A NA study, sponsored by Thomas Jefferson University.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT00371046 is a NA study that has completed, run by Thomas Jefferson University. The registered enrollment target is 100 participants.
The verdict
NCT00371046, a NA study, has completed, sponsored by Thomas Jefferson University.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study Summary
The objective of this study is to investigate the effect of the use of both sonographic cervical length (CL) and fetal fibronectin (FFN) on the length of outpatient triage and preterm labor interventions in symptomatic women with intact membranes. We performed a randomized trial of the use of transvaginal ultrasound cervical length and fetal fibronectin in women being evaluated for suspected PTL at a gestational age between 24 and 33 weeks 6 days. Women are randomized to either a standard (blinded) or a protocol arm. Women in the standard arm are evaluated without the results of the CL and FFN while women in the protocol arm are evaluated using the results of the CL and FFN and managing physicians are asked to follow a specific PTL algorithm to determine a women's eligibility for treatment. The primary outcome is length of stay in the triage area before discharge.
Interventions
- PROCEDURE Transvaginal ultrasound cervical length
- PROCEDURE Cervicovaginal fetal fibronectin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2003-10 |
| Est. Completion | 2006-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00371046
The ClinicalTrials.gov registry entry for NCT00371046 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Thomas Jefferson University, which has 292 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Transvaginal ultrasound cervical length is the first listed.
NCT00371046 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00371046 about?
NCT00371046 is a clinical study titled "Does Fetal Fibronectin and Ultrasound Cervical Length Help in the Evaluation of Women With Suspected Preterm Labor?". The objective of this study is to investigate the effect of the use of both sonographic cervical length (CL) and fetal fibronectin (FFN) on the length of outpatient triage and preterm labor interventions in symptomatic women with intact membranes. We performed a randomized trial of the use of trans...
What is the current status of trial NCT00371046?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2003-10. Estimated completion is 2006-12.
What interventions are being tested in trial NCT00371046?
The interventions under investigation include: Transvaginal ultrasound cervical length (PROCEDURE), Cervicovaginal fetal fibronectin (PROCEDURE).
Who is sponsoring clinical trial NCT00371046?
This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.
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