Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04797585 · ClinicalTrials.gov registry record · NA
Vaginal Hysterectomy vs Supracervical Hysterectomy at the Time of Sacrocolpopexy
A NA study, sponsored by The Cleveland Clinic.
- Terminated
- Registry status
- NA
- Development phase
- 3
- Enrollment target
NCT04797585: Clinical Trial NA study, sponsored by The Cleveland Clinic.
NCT04797585 is a NA study that was terminated before completion, run by The Cleveland Clinic. The registered enrollment target is 3 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04797585, a NA study, was terminated before completion, sponsored by The Cleveland Clinic.
- TERMINATED
- Registry status
- NA
- Development phase
- 3 participants
- Enrollment target
Study Summary
The primary objective of the proposed study is to determine the difference in surgical time between minimally invasive (laparoscopic) sacrocolpopexy performed with concurrent vaginal hysterectomy versus laparoscopic supracervical hysterectomy. The secondary objectives are to determine if there are differences in intraoperative adverse events and postoperative mesh-related complications and prolapse recurrence between the groups.
Primary Outcome
Completion = time of abdominal incisions closed
Interventions
- OTHER Laparoscopic supracervical hysterectomy
- OTHER Vaginal hysterectomy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 3 participants |
| Start Date | 2021-03-16 |
| Est. Completion | 2023-09-12 |
| Phase | NA |
Why NCT04797585 stopped before completion
NCT04797585 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 2 interventions - of which Laparoscopic supracervical hysterectomy is the first listed.
NCT04797585 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04797585 about?
NCT04797585 is a clinical study titled "Vaginal Hysterectomy vs Supracervical Hysterectomy at the Time of Sacrocolpopexy". The primary objective of the proposed study is to determine the difference in surgical time between minimally invasive (laparoscopic) sacrocolpopexy performed with concurrent vaginal hysterectomy versus laparoscopic supracervical hysterectomy. The secondary objectives are to determine if there are d...
What is the current status of trial NCT04797585?
This trial is currently terminated. It is a NA study. The enrollment target is 3 participants. The study started on 2021-03-16. Estimated completion is 2023-09-12.
What interventions are being tested in trial NCT04797585?
The interventions under investigation include: Laparoscopic supracervical hysterectomy (OTHER), Vaginal hysterectomy (OTHER).
Who is sponsoring clinical trial NCT04797585?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04797585's enrollment target sits among peer trials
3 1996th of 2000 higher than 4 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 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