Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01405703 · ClinicalTrials.gov registry record
Percutaneous Versus Open Plate Fixation of Diaphyseal Clavicle Fractures
A clinical trial, sponsored by University of Utah.
- Completed
- Registry status
- 35
- Enrollment target
NCT01405703: Completed study, sponsored by University of Utah.
NCT01405703 is a clinical trial that has completed, run by University of Utah. The registered enrollment target is 35 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01405703 has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- 35 participants
- Enrollment target
Study Summary
This is a prospective, level II evidence comparison between two cohorts. This study is designed to compare the percutaneous versus open approach for plate fixation of diaphyseal clavicle fractures. This study includes questionnaires and measurements that will collect data on incision-related numbness, union rates, overall outcomes, complication rates of the two methods, infection rates, and overall satisfaction. The surgical procedure, all radiographs and follow-up visits to a minimum of one year are the principle investigators (PI's) standard of care for this injury. Measurements and questionnaires are related to the study.
Primary Outcome
The primary outcome measure for this study will be incision related numbness, based on clinical examination and the use of our skin numbness map. Our null hypothesis is that there will be no difference in incision related numbness between the two groups: percutaneous versus open approach. Our primary objective is to disprove this hypothesis, predicting that the percutaneously treated group will have less incisional numbness.
Interventions
- OTHER xrays
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2011-07 |
| Est. Completion | 2015-05 |
What the finished NCT01405703 record still lists
NCT01405703 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 35 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which xrays is the first listed.
NCT01405703 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01405703 about?
NCT01405703 is a clinical study titled "Percutaneous Versus Open Plate Fixation of Diaphyseal Clavicle Fractures". This is a prospective, level II evidence comparison between two cohorts. This study is designed to compare the percutaneous versus open approach for plate fixation of diaphyseal clavicle fractures. This study includes questionnaires and measurements that will collect data on incision-related numbnes...
What is the current status of trial NCT01405703?
This trial is currently completed. The enrollment target is 35 participants. The study started on 2011-07. Estimated completion is 2015-05.
What interventions are being tested in trial NCT01405703?
The interventions under investigation include: xrays (OTHER).
Who is sponsoring clinical trial NCT01405703?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
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
- NCT01697371 · 35 participants · NA
Proton Therapy in the Treatment of Liver Metastases
- NCT01940757 · 35 participants · Phase 1
Experimental Infection of Hookworm-naïve Adults With Dermally-applied Infectious Necator Americanus Hookworm Larvae
- NCT02235857 · 35 participants · NA
Post Approval Study of Liposorber LA-15 System for the Treatment of Focal Segmental Glomerulosclerosis in Children
- NCT02637934 · 35 participants · Phase 1
Phase I Pilot Study of Biodistribution, Metabolism and Excretion of Novel Radiotracer [18F]Fluorthanatrace (FTT) by PET/CT
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