Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT03752073 · ClinicalTrials.gov registry record · NA
Comparison of Two Mechanical Methods of Outpatient Ripening of the Cervix
A NA study, sponsored by Ochsner Health System.
- Terminated
- Registry status
- NA
- Development phase
- 185
- Enrollment target
NCT03752073: Clinical Trial NA study, sponsored by Ochsner Health System.
NCT03752073 is a NA study that was terminated before completion, run by Ochsner Health System. The registered enrollment target is 185 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03752073, a NA study, was terminated before completion, sponsored by Ochsner Health System.
- TERMINATED
- Registry status
- NA
- Development phase
- 185 participants
- Enrollment target
Study Summary
This is a randomized prospective trial of two mechanical methods of pre-induction cervical ripening agents.
Primary Outcome
Time in minutes from placement of cervical ripening agent to delivery
Interventions
- DEVICE Trans-cervical cervical balloon
- DEVICE Hygroscopic cervical dilator
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 185 participants |
| Start Date | 2019-03-01 |
| Est. Completion | 2023-01-01 |
| Phase | NA |
Why NCT03752073 stopped before completion
NCT03752073 is an interventional study that assigns participants to a tested intervention. The registered 185 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower).
The record links to 0 conditions, and to 2 interventions - of which Trans-cervical cervical balloon is the first listed.
NCT03752073 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03752073 about?
NCT03752073 is a clinical study titled "Comparison of Two Mechanical Methods of Outpatient Ripening of the Cervix". This is a randomized prospective trial of two mechanical methods of pre-induction cervical ripening agents.
What is the current status of trial NCT03752073?
This trial is currently terminated. It is a NA study. The enrollment target is 185 participants. The study started on 2019-03-01. Estimated completion is 2023-01-01.
What interventions are being tested in trial NCT03752073?
The interventions under investigation include: Trans-cervical cervical balloon (DEVICE), Hygroscopic cervical dilator (DEVICE).
Who is sponsoring clinical trial NCT03752073?
This trial is sponsored by Ochsner Health System, which has 29 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03752073's enrollment target sits among peer trials
185 580th of 2000 higher than 1,420 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT04041154 · 185 participants · NA
Behavioral and Neural Representations of Subjective Effort Cost
- NCT04484272 · 185 participants · NA
A Stress and Pain Self-management m-Health App for Adult Outpatients With Sickle Cell Disease
- NCT05020860 · 185 participants · Phase 2
Correlation of Clinical Response to Pathologic Response in Patients With Early Breast Cancer
- NCT05793541 · 185 participants · NA
Just-in-time Interventions for Reducing Short-term Suicide Risk
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI