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NCT05506631 · ClinicalTrials.gov registry record · NA
Foley Balloon Study for Cervical Ripening - Cost Comparison Between Outpatient and Inpatient Cervical Ripening
A NA study, sponsored by Lehigh Valley Hospital.
- Completed
- Registry status
- NA
- Development phase
- 140
- Enrollment target
NCT05506631 is a NA study that has completed, run by Lehigh Valley Hospital. The registered enrollment target is 140 participants.
The verdict
NCT05506631, a NA study, has completed, sponsored by Lehigh Valley Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 140 participants
- Enrollment target
Study Summary
The objective of this study is to determine the impact of outpatient cervical ripening with transcervical balloon placement for induction of labor at term on the length and cost of inpatient hospitalization when compared to inpatient cervical ripening.
Interventions
- PROCEDURE Outpatient Foley balloon placement
- PROCEDURE Inpatient Foley Balloon placement
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 140 participants |
| Start Date | 2021-11-01 |
| Est. Completion | 2024-10-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05506631
The ClinicalTrials.gov registry entry for NCT05506631 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Lehigh Valley Hospital, which has 16 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Outpatient Foley balloon placement is the first listed.
NCT05506631 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05506631 about?
NCT05506631 is a clinical study titled "Foley Balloon Study for Cervical Ripening - Cost Comparison Between Outpatient and Inpatient Cervical Ripening". The objective of this study is to determine the impact of outpatient cervical ripening with transcervical balloon placement for induction of labor at term on the length and cost of inpatient hospitalization when compared to inpatient cervical ripening.
What is the current status of trial NCT05506631?
This trial is currently completed. It is a NA study. The enrollment target is 140 participants. The study started on 2021-11-01. Estimated completion is 2024-10-30.
What interventions are being tested in trial NCT05506631?
The interventions under investigation include: Outpatient Foley balloon placement (PROCEDURE), Inpatient Foley Balloon placement (PROCEDURE).
Who is sponsoring clinical trial NCT05506631?
This trial is sponsored by Lehigh Valley Hospital, which has 16 total clinical trials registered on ClinicalTrials.gov.
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