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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: Completed NA study, sponsored by The University of Texas Health Science Center, Houston.
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, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
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).
Primary Outcome
The time taken to complete an Open Reduction Internal Fixation (ORIF) \[referred to as the "plating time"\] was defined as beginning after dissection was complete and fractures were initially reduced, and ending after all fracture sites were fixated with the final screw placed.
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 |
What the finished NCT04283981 record still lists
NCT04283981 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 2 interventions - of which Control group without use of VSP is the first listed.
NCT04283981 does not publish any study locations in the registry export this page uses.
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
How this trial's enrollment target compares
Where NCT04283981's enrollment target sits among peer trials
28 1704th of 2000 higher than 293 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
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