Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04283981 · ClinicalTrials.gov registry record · NA
Comparison of Operating Room Time Length With the Use of Virtual Surgical Planning Versus Conventional Treatment of Mandible Fractures
A NA study, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- NA
- Development phase
- 28
- Enrollment target
NCT04283981 is a NA study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 28 participants.
The verdict
NCT04283981, a NA study, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- NA
- Development phase
- 28 participants
- Enrollment target
Study Summary
The purpose of this trial is to compare operating room time between conventional treatment techniques \[without Virtual surgical Planning (VSP)\] versus treatment with use of Virtual surgical Planning (VSP) in patients that undergo mandibular reconstruction via open reduction internal fixation (ORIF).
Interventions
- DEVICE Control group without use of VSP
- DEVICE Treatment Group with use of VSP
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2021-01-24 |
| Est. Completion | 2022-11-10 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04283981
The ClinicalTrials.gov registry entry for NCT04283981 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Control group without use of VSP is the first listed.
NCT04283981 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04283981 about?
NCT04283981 is a clinical study titled "Comparison of Operating Room Time Length With the Use of Virtual Surgical Planning Versus Conventional Treatment of Mandible Fractures". The purpose of this trial is to compare operating room time between conventional treatment techniques \[without Virtual surgical Planning (VSP)\] versus treatment with use of Virtual surgical Planning (VSP) in patients that undergo mandibular reconstruction via open reduction internal fixation (ORIF...
What is the current status of trial NCT04283981?
This trial is currently completed. It is a NA study. The enrollment target is 28 participants. The study started on 2021-01-24. Estimated completion is 2022-11-10.
What interventions are being tested in trial NCT04283981?
The interventions under investigation include: Control group without use of VSP (DEVICE), Treatment Group with use of VSP (DEVICE).
Who is sponsoring clinical trial NCT04283981?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.