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Recruiting NCT07523802

NCT07523802 Management of Postoperative Pain Following Free Gingival Graft Harvesting Using Ora-Aid Versus Acrylic Palatal Stent

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Clinical Trial Summary
NCT ID NCT07523802
Status Recruiting
Phase
Sponsor Cairo University
Condition Postoperative Pain
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2026-01-14
Primary Completion 2026-07-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Ora-Aid Oral Wound DressingAcrylic Resin Palatal Stent

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 20 participants in total. It began in 2026-01-14 with a primary completion date of 2026-07-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized clinical trial evaluates the effectiveness of Ora-Aid oral wound dressing compared to an acrylic palatal stent in managing postoperative pain following free gingival graft harvesting. Patients undergoing graft harvesting will be randomly assigned to receive either Ora-Aid dressing or a palatal stent at the donor site. The primary outcome is postoperative pain assessed using the Visual Analogue Scale (VAS). Secondary outcomes include analgesic consumption, wound size, patient satisfaction, and color match over a 42-day follow-up period.

Eligibility Criteria

Inclusion Criteria: * Patient over 18 years of age * Systemically healthy * Patients with good oral hygiene * Patients with mucogingival defects scheduled for free gingival graft (FGG) Exclusion Criteria: * Pregnancy or breastfeeding * Severe gagging reflex * Smokers * Patients allergic to the materials used in the study

Frequently Asked Questions

Who can join the NCT07523802 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Postoperative Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07523802 currently recruiting?

Yes, NCT07523802 is actively recruiting participants. Visit ClinicalTrials.gov or contact Cairo University to inquire about joining.

Where is the NCT07523802 trial being conducted?

This trial is being conducted at Cairo, Egypt.

Who is sponsoring the NCT07523802 clinical trial?

NCT07523802 is sponsored by Cairo University. The trial plans to enroll 20 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology