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Various Procedural Treatment Options for Androgenetic Alopecia

S

Sheikh Zayed Medical College

Status and phase

Not yet enrolling
Phase 2

Conditions

Androgenetic Alopecia

Treatments

Drug: Topical minoxidil
Drug: topical finasteride

Study type

Interventional

Funder types

Other

Identifiers

NCT06826001
sheikh-ZMC-FH

Details and patient eligibility

About

Androgenetic alopecia (AGA)is the most common form of alopecia. It predominantly affects males, but there has been a significant surge in female preponderance too, over the last decade Minoxidil belong to the anti-hypertensive class but it also affects the potassium channels present in vascular smooth muscles and hair follicles. This potassium channel activity may stimulate the microcirculation around the hair follicles and induces arteriolar vasodilation, thereby encouraging conditions conducive to hair growth Topical administration of finasteride offers the potential to reduce systemic effects related to its mechanism of action by preferentially inhibiting 5-a reductase in the scalp, as has been suggested in recent years so in this study we are going to compare efficacy of topical minoxidil versus topical finasteride in treatment of androgenetic alopecia

Full description

Androgenetic alopecia (AGA)is considered to be a very common form of alopecia. Minoxidil belong to the anti-hypertensive class but it also affects the potassium channels present in vascular smooth muscles and hair follicles. This potassium channel activity may stimulate the microcirculation around the hair follicles and induces arteriolar vasodilation, thereby encouraging conditions conducive to hair growth The clinical efficacy of oral finasteride for treating AGA is well established. Although oral finasteride is generally well tolerated Topical finasteride is a medication that is used to treat hair loss in men and women. It is a topical version of the oral medication finasteride, which works by blocking the conversion of testosterone to dihydrotestosterone (DHT), a hormone that contributes to hair loss. Topical administration of finasteride offers the potential to reduce systemic effects related to its mechanism of action by preferentially inhibiting 5-a reductase in the scalp, as has been suggested in recent years.

OBJECTIVE "To compare the efficacy of topical finasteride vs topical minoxidil in the treatment of androgenetic alopecia in tertiary care hospital"

DATA COLLECTION:

Data will be collected on prescribed proforma which is attached, at Dermatology OPD, Sheikh Zayed Hospital, Rahim Yar Khan. Patient will be selected on basis of inclusion & exclusion criteria. Informed consent will be taken from selected patients before data collection. Study will include 190 patients which will be divided into 2 groups A & B, 95 in each group. Group A will receive topical finasteride spray 0.25% twice daily for 12 weeks. Group B will receive topical 5% minoxidil twice daily for 12 weeks Patient will be followed at the end of 12 weeks therapy.

DATA ANALYSIS:

Data will be analyzed by SPSS (Statistical Package for the Social Sciences) v25.0.

Enrollment

190 estimated patients

Sex

Male

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age: 20-50 years
  • Gender: Male
  • ANDROGENETIC ALOPECIA with AGA stage 2-6 Norwood-Hamilton -classification
  • Patients not taking any treatment in last 1 month

Exclusion criteria

  • Abrasion or abnormalities to the scalp
  • Hair transplant
  • Hypersensitivity
  • Recent history of local infections of the head
  • History of relevant significant disease active seborrheic dermatitis
  • Concurrent use of :
  • corticosteroids
  • anabolic steroids or over-the-counter 'hair restorers'
  • use of drugs with anti-androgenic properties within 6 months light or laser treatment of the scalp within the last 3 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

190 participants in 2 patient groups

Finesteride group
Active Comparator group
Description:
Group A will receive topical finasteride spray 0.25% twice daily for 12 weeks
Treatment:
Drug: topical finasteride
Minoxidil group
Active Comparator group
Description:
Group B will receive topical 5% minoxidil twice daily for 12 weeks
Treatment:
Drug: Topical minoxidil

Trial contacts and locations

1

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Central trial contact

Farah Humera, post graduate resident derma

Data sourced from clinicaltrials.gov

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