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NCT06892496 · ClinicalTrials.gov registry record · NA
Patient-reported Outcomes of Donor Site Healing Using Different Palatal Protection Techniques
A NA study of Gingival Recession and Mucosal Erosion, sponsored by Virginia Commonwealth University.
- Recruiting
- Registry status
- NA
- Development phase
- 42
- Enrollment target
- 1
- Study location
NCT06892496 is a NA study of Gingival Recession and Mucosal Erosion that is actively recruiting participants, run by Virginia Commonwealth University. The registered enrollment target is 42 participants, above the 29-participant average among 10 other Gingival Recession trials with a reported enrollment target (45% higher). The trial reports 1 study location across 1 state.
The verdict
NCT06892496, a NA study of Gingival Recession and Mucosal Erosion, is actively recruiting participants, sponsored by Virginia Commonwealth University.
- RECRUITING
- Registry status
- NA
- Development phase
- 42 participants
- Enrollment target
- 1
- Study location
Study Summary
This study has been initiated to evaluate the question, "What is the best way to protect the palate after a gum graft is removed?" The overall objective is to determine if there is a difference in PROMs of donor site healing using different palatal post-operative protection techniques.
Conditions Studied
Interventions
- OTHER Visual Analog scale (VAS) questionnaire
- OTHER Vacuum-formed retainer (VFR) technique
- OTHER 3-D printed acrylic resin stent (3DS) technique
- OTHER Flowable resin composite stent (FRC) technique
- OTHER Photographs of the patient's palate
Study Locations (1)
Virginia
- Virginia Commonwealth University - Richmond
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Start Date | 2025-03-07 |
| Est. Completion | 2026-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06892496
The ClinicalTrials.gov registry entry for NCT06892496 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 42 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 29-participant average among 10 other Gingival Recession trials with a reported enrollment target (45% higher). The listed sponsor is Virginia Commonwealth University, which has 558 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Gingival Recession appearing as the primary indexed condition, and to 5 interventions - of which Visual Analog scale (VAS) questionnaire is the first listed.
NCT06892496 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.
Frequently Asked Questions
What is clinical trial NCT06892496 about?
NCT06892496 is a clinical study titled "Patient-reported Outcomes of Donor Site Healing Using Different Palatal Protection Techniques". This study has been initiated to evaluate the question, "What is the best way to protect the palate after a gum graft is removed?" The overall objective is to determine if there is a difference in PROMs of donor site healing using different palatal post-operative protection techniques.
What is the current status of trial NCT06892496?
This trial is currently recruiting. It is a NA study. The enrollment target is 42 participants. The study started on 2025-03-07. Estimated completion is 2026-07.
What conditions does trial NCT06892496 study?
This clinical trial studies the following conditions: Gingival Recession, Mucosal Erosion.
What interventions are being tested in trial NCT06892496?
The interventions under investigation include: Visual Analog scale (VAS) questionnaire (OTHER), Vacuum-formed retainer (VFR) technique (OTHER), 3-D printed acrylic resin stent (3DS) technique (OTHER), Flowable resin composite stent (FRC) technique (OTHER), Photographs of the patient's palate (OTHER).
Who is sponsoring clinical trial NCT06892496?
This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06892496 being conducted?
This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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