CTRI/2018/03/012591
Recruiting
N/A
To study the efficacy and safety of intra-operative use of Platelet rich plasma(PRP) in autologous non cultured epidermal cell suspension (NCECS) grafting when compared to autologous non cultured epidermal cell suspension alone in surgical management of stable vitiligo. - NCS-PRP
Intitutional research committee0 sites0 target enrollmentTBD
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Stable Vitiligo
- Sponsor
- Intitutional research committee
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with stable Vitilgo with no increase in size of lesion for past 06 months
Exclusion Criteria
- •1\) Unstable vitiligo (New lesion or extension of pre\-existing lesion)
- •2\) Vitiligo stabilized on systemic medical therapy
- •3\) Evidence or history of keloid/hypertrophic scars.
- •4\) Patients with chronic auto immune and infectious diseases e.g. DM, Thyroid disease, HTN, Hep B,C,HIV etc.
- •5\) Patients with bleeding disorders or on medications affecting platelet function e.g. Ecosprin.
Outcomes
Primary Outcomes
Not specified
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