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OPEN LABEL, NON RANDOMIZED, PLACEBO-CONTROLLED STUDY OF PLATELET RICH PLASMA (PRP) IN ALOPECIA, STRAIE AND ATROPHIC ACNE SCAR.

OPEN LABEL, NON RANDOMIZED, PLACEBO-CONTROLLED STUDY OF PLATELET RICH PLASMA (PRP) IN ALOPECIA, STRAIE AND ATROPHIC ACNE SCAR. - -

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/09/003976
Enrollment
20
Registered
2013-09-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- alopecia, atrophic acne scars, striae

Interventions

Intervention1: autologus platelet rich plasma(PRP) dose: 4 ml( 9 part PRP with 1 part sterile calcium gluconate) frequency: once monthly route of administration: intradermal: autologus platelet rich

Sponsors

Gujarat Cancer Society Medical college hospital and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients between ages of 18 to 70 years. 2. Patients with androgenic alopecia or scaring alopecia who are not taking any other treatment. 3. Patients with atrophic scars >1 in no. and not taking any other treatment. 4. Patients with straie >1 in no. 5. Otherwise healthy patients. 6. Non-pregnant, non-lactating women

Exclusion criteria

Exclusion criteria: 1. Patients below age of 18 or above the age of 70 yr. 2. Patients who were on oral isotretinoin in last 6 months. 3. Patients who underwent any surgical modality of treatment in last 2 month. 4. Patients who have history of keloid formation or koebnerization for vitiligo. 5. Patients with atrophic scars or striae 6. Patients who are on oral immunosuppressive drugs. 7. Patients having history of any systemic diseases like- renal disease, liver disease, diabetes, tuberculosis, HIV etc.

Design outcomes

Primary

MeasureTime frame
alopecia primary outcome: increase in hair density, increase hair growth. acne scar primary outcome:rejuvenation of acne scars,decrease depth of scars striae:decrease in thickness and length, decrease erythemaTimepoint: every month for six months

Secondary

MeasureTime frame
adverse events, minimum time duration for starting and maximum effects.Timepoint: every month for six months

Countries

India

Contacts

Public ContactDr Jigna Padhiyar

GCS Medical College, hospital and research centre

patelnayan78.np@gmail.com9925011309

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026