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RECRUITING NA

Patient-reported Outcomes of Donor Site Healing Using Different Palatal Protection Techniques

NCT06892496 · View on ClinicalTrials.gov ↗

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.

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

FieldValue
Enrollment Target 42 participants
Start Date 2025-03-07
Est. Completion 2026-07
Phase NA

Sponsor

Virginia Commonwealth University

513 total trials

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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. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 42 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Virginia Commonwealth University, which has 513 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06892496 reports 1 study location spanning 1 distinct geographic area — top geographies include Virginia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

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). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06892496?

This trial is sponsored by Virginia Commonwealth University, which has 513 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial