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NCT02606643 · ClinicalTrials.gov registry record · NA
Balloon Catheter for Cervical Ripening
A NA study, sponsored by St. Louis University.
- Completed
- Registry status
- NA
- Development phase
- 134
- Enrollment target
NCT02606643 is a NA study that has completed, run by St. Louis University. The registered enrollment target is 134 participants.
The verdict
NCT02606643, a NA study, has completed, sponsored by St. Louis University.
- COMPLETED
- Registry status
- NA
- Development phase
- 134 participants
- Enrollment target
Study Summary
Once admitted, women who will have a transcervical balloon catheter inserted for induction will be approached for participation in this study. If they agree to be take part in this study (tape or no tape) they will be randomized into the study. After the balloon catheter is inserted, the balloon will then be filled with approximately 50-60 mL of normal saline, this is normal procedure. Study related: If randomized to "No Taping" the foley will be positioned comfortable and not placed to tension. For the "Tension" arm, tension will be placed on the balloon catheter, which will then be taped to the patient's inner thigh. The tension will be assessed and retaped as needed approximately every 30 minutes by the research and/or the nursing staff.
Interventions
- PROCEDURE Slight traction
- PROCEDURE Foley Catheter to no traction
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 134 participants |
| Start Date | 2014-10 |
| Est. Completion | 2016-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02606643
The ClinicalTrials.gov registry entry for NCT02606643 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 134 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Louis University, which has 107 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Slight traction is the first listed.
NCT02606643 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02606643 about?
NCT02606643 is a clinical study titled "Balloon Catheter for Cervical Ripening". Once admitted, women who will have a transcervical balloon catheter inserted for induction will be approached for participation in this study. If they agree to be take part in this study (tape or no tape) they will be randomized into the study. After the balloon catheter is inserted, the balloon wil...
What is the current status of trial NCT02606643?
This trial is currently completed. It is a NA study. The enrollment target is 134 participants. The study started on 2014-10. Estimated completion is 2016-11.
What interventions are being tested in trial NCT02606643?
The interventions under investigation include: Slight traction (PROCEDURE), Foley Catheter to no traction (PROCEDURE).
Who is sponsoring clinical trial NCT02606643?
This trial is sponsored by St. Louis University, which has 107 total clinical trials registered on ClinicalTrials.gov.
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