# Topical CBD Scar Healing Study

> **NCT06129591** · PHASE1 · NOT_YET_RECRUITING · sponsor: **University of Oklahoma** · enrollment: 22 (estimated)

## Conditions studied

- Paramedian Forehead Flap

## Interventions

- **DRUG:** Vantage Hemp CBD Isolate + Silicone patch
- **DRUG:** Silicone patch

## Key facts

- **NCT ID:** NCT06129591
- **Lead sponsor:** University of Oklahoma
- **Sponsor class:** OTHER
- **Phase:** PHASE1
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-05
- **Primary completion:** 2027-07
- **Final completion:** 2028-07
- **Target enrollment:** 22 (ESTIMATED)
- **Last updated:** 2026-03-05


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06129591

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06129591, "Topical CBD Scar Healing Study". Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/clinical/NCT06129591. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
