๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-04

Patient-reported Outcomes of Donor Site Healing Using Different Palatal Protection Techniques (NCT06892496)

Patient-reported Outcomes of Donor Site Healing Using Different Palatal Protection Techniques: a Randomized Controlled Clinical Trial

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿ“‹ Clinical Research Protocol Sponsor: Virginia Commonwealth University

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Virginia Commonwealth University โ€” Richmond, Virginia

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • 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)
  • Measuring graft dimensions (OTHER)
  • Chairside Polymer Stent (OTHER)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • Virginia Commonwealth University โ€” Richmond, Virginia

๐Ÿ“ž Contact the Study Coordinator

Phone: (804) 628-8377

Email: amorimcavalr@vcu.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Mucosal Erosion clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—