# Topical CBD Scar Outcomes Study

> **NCT05650697** · EARLY_PHASE1 · NOT_YET_RECRUITING · sponsor: **University of Oklahoma** · enrollment: 22 (estimated)

## Conditions studied

- Forehead; Wound

## Interventions

- **BIOLOGICAL:** Group 1 cannabidiol (CBD) with silicone ointment
- **BIOLOGICAL:** Group 2 silicone patch

## Key facts

- **NCT ID:** NCT05650697
- **Lead sponsor:** University of Oklahoma
- **Sponsor class:** OTHER
- **Phase:** EARLY_PHASE1
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-09
- **Primary completion:** 2027-12
- **Final completion:** 2027-12
- **Target enrollment:** 22 (ESTIMATED)
- **Last updated:** 2026-04-01


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05650697

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05650697, "Topical CBD Scar Outcomes Study". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT05650697. Licensed CC0.

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