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Clinical Trials/CTRI/2018/05/014113
CTRI/2018/05/014113
Completed
Phase 2

Role of platelet rich plasma (PRP) in the treatment of male type baldness

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Institute of Medical sciences Banaras Hindu University
Enrollment
80
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
February 24, 2018
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.All the patients not using topical minoxidil and finasteride for at least 6 months will be considered for PRP therapy.
  • 2\.Age group 20 â?? 60 years
  • 3\.Sex\- Male
  • 4\.Mild to moderate AGA (Hamilton\-Norwood score II\-V) .
  • 5\.Patients willing to come for follow up every month for 5 months.

Exclusion Criteria

  • 1\.Patients not giving informed written consent, unable to understand the protocol and uncooperative patients.
  • 2\.Any inflammation, erythema or scarring over scalp except mild seborrheic dermatitis.
  • 3\.Patients who have history of malignancies, platelets disorders or bleeding disorders, anemia ( haemoglobulin of less than 10 gm/dl), bone marrow aplasia, diabetes, sepsis, and cancer.
  • 4\.Patients taking theses any of these medications\-
  • i.Anti\-coagulants â?? heparin, warfarin
  • ii.Anti\-hypertensives â?? beta\-blockers, ACE inhibitors hormones
  • iii.Anticonvulsants â?? valproic acid, carbamazepine, phenytoin, mood stabilizers Antidepressants, lithium
  • iv.Aspirin or any non\-steroidal anti\-inflammatory drugs two week prior to procedure.
  • v.Other medications cimetidine, retinoids (acitretin \> isotretinoin), antithyroid drugs, cholesterol lowering drugs, interferons, amphetamines, bromocriptine, levodopa, some antipsychotic and anti\-anxiety drugs, rarely tricyclic antidepressants such as amitriptyline
  • 5\.Patients who are known to be HIV, hepatitis B or C positive or otherwise immunocompromised.

Outcomes

Primary Outcomes

Not specified

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