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Clinical Trials/CTRI/2018/03/012591
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Intitutional research committee

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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