Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT07189156 · ClinicalTrials.gov registry record · NA
Weight Bearing After Pelvis and Acetabulum Fracture Fixation
A NA study, sponsored by University of Mississippi Medical Center.
- Not yet
- Registry status
- NA
- Development phase
- 200
- Enrollment target
NCT07189156: Clinical Trial NA study, sponsored by University of Mississippi Medical Center.
NCT07189156 is a NA study that has not yet begun recruiting, run by University of Mississippi Medical Center. The registered enrollment target is 200 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07189156, a NA study, has not yet begun recruiting, sponsored by University of Mississippi Medical Center.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
Study Summary
The goal of this study to determine if a randomized clinical trial of immediate versus delayed weight bearing after undergoing surgical fixation of a pelvis or acetabulum fracture is feasible. The main questions it aims to answer are: Are surgeons willing to allow inclusion of their patients into such a trial? Are patients willing to participate in such a trial? Will patients be compliant with assigned weight bearing status in such a trial? Can good patient follow-up be obtained in such a trial? Is participation in such a trial safe? Patients from 7 medical centers will be enrolled, and randomized to immediate weight bearing as tolerated (WBAT) versus delayed WBAT (for 6-12 weeks). Feasibility metrics revolving around enrollment, follow-up, and documentation will be monitored, as well as medical and surgical complications. This pilot study will help inform feasibility and design of a larger definitive multicenter randomized controlled trial (RCT) on this topic.
Primary Outcome
Target enrollment of 50% of patients (surgeon agreement to enroll patient) and 50% of patients eligible for inclusion to agree to participate in study
Interventions
- OTHER Immediate Weight Bearing Pelvis
- OTHER Delayed Weight Bearing Pelvis
- OTHER Immediate Weight Bearing Acetabulum
- OTHER Delayed Weight Bearing Acetabulum
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2025-10 |
| Est. Completion | 2028-12 |
| Phase | NA |
What is known before NCT07189156 opens enrollment
NCT07189156 is an interventional study that assigns participants to a tested intervention. The registered 200 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 (86% lower).
The record links to 0 conditions, and to 4 interventions - of which Immediate Weight Bearing Pelvis is the first listed.
NCT07189156 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07189156 about?
NCT07189156 is a clinical study titled "Weight Bearing After Pelvis and Acetabulum Fracture Fixation". The goal of this study to determine if a randomized clinical trial of immediate versus delayed weight bearing after undergoing surgical fixation of a pelvis or acetabulum fracture is feasible. The main questions it aims to answer are: Are surgeons willing to allow inclusion of their patients into s...
What is the current status of trial NCT07189156?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2025-10. Estimated completion is 2028-12.
What interventions are being tested in trial NCT07189156?
The interventions under investigation include: Immediate Weight Bearing Pelvis (OTHER), Delayed Weight Bearing Pelvis (OTHER), Immediate Weight Bearing Acetabulum (OTHER), Delayed Weight Bearing Acetabulum (OTHER).
Who is sponsoring clinical trial NCT07189156?
This trial is sponsored by University of Mississippi Medical Center, which has 96 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07189156's enrollment target sits among peer trials
200 506th of 2000 higher than 1,434 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
- NCT00107289 · 200 participants · Phase 2
Iodine I 131 Metaiodobenzylguanidine in Treating Patients With Recurrent, Progressive, or Refractory Neuroblastoma or Malignant Pheochromocytoma or Paraganglioma
- NCT00109174 · 200 participants · NA
MRS Measurement of Glutamate and GABA Metabolism in Brain
- NCT00177268 · 200 participants
Blood, Urine, and Tissue Collection for Cutaneous Lymphoma, Eczema, and Atopic Dermatitis Research
- NCT00493688 · 200 participants
A Study to Determine Whether Perioperative Energy Dynamics Correlates With Postoperative Outcomes
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia