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NCT01063244 · ClinicalTrials.gov registry record · Phase 3
Comparison of Foley Balloon With or Without Traction for the Cervical Ripening
A Phase 3 study of Pregnancy, sponsored by St. Luke's Hospital, Pennsylvania.
- Completed
- Registry status
- Phase 3
- Development phase
- 65
- Enrollment target
- 1
- Study location
NCT01063244 is a Phase 3 study of Pregnancy that has completed, run by St. Luke's Hospital, Pennsylvania. The registered enrollment target is 65 participants, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01063244, a Phase 3 study of Pregnancy, has completed, sponsored by St. Luke's Hospital, Pennsylvania.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 65 participants
- Enrollment target
- 1
- Study location
Study Summary
We will compare the use of foley bulb catheters placed in the cervix for ripening of the cervix for labor induction,.
Conditions Studied
Interventions
- DEVICE foley balloon only
- DEVICE foley balloon with weight attached
Study Locations (1)
Pennsylvania
- St Luke's Hosptial & Health Network - Bethlehem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2009-01 |
| Est. Completion | 2012-01 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01063244
The ClinicalTrials.gov registry entry for NCT01063244 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 65 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (93% lower). The listed sponsor is St. Luke's Hospital, Pennsylvania, which has 10 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pregnancy appearing as the primary indexed condition, and to 2 interventions - of which foley balloon only is the first listed.
NCT01063244 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT01063244 about?
NCT01063244 is a clinical study titled "Comparison of Foley Balloon With or Without Traction for the Cervical Ripening". We will compare the use of foley bulb catheters placed in the cervix for ripening of the cervix for labor induction,.
What is the current status of trial NCT01063244?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 65 participants. The study started on 2009-01. Estimated completion is 2012-01.
What conditions does trial NCT01063244 study?
This clinical trial studies the following conditions: Pregnancy.
What interventions are being tested in trial NCT01063244?
The interventions under investigation include: foley balloon only (DEVICE), foley balloon with weight attached (DEVICE).
Who is sponsoring clinical trial NCT01063244?
This trial is sponsored by St. Luke's Hospital, Pennsylvania, which has 10 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01063244 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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