Topical Finasteride vs Minoxidil for Androgenetic Alopecia
topical finasteride
+ Topical minoxidil
Alopecia+4
+ Hair Diseases
+ Hypotrichosis
Treatment Study
Summary
Study start date: February 1, 2025
Actual date on which the first participant was enrolled.This clinical trial aims to compare the effectiveness of two different topical treatments, finasteride and minoxidil, for addressing androgenetic alopecia, a common type of hair loss affecting both men and women. Traditionally, finasteride is taken orally to block a hormone linked to hair loss, but this study uses it as a topical spray to potentially minimize side effects by targeting the scalp directly. Minoxidil is another topical treatment that helps improve blood flow around hair follicles, encouraging hair growth. The study's goal is to explore which of these treatments is more effective in promoting hair growth, offering valuable insights for those struggling with hair loss. Participants in this study are divided into two groups, each consisting of 95 patients. One group receives a finasteride spray applied to the scalp twice a day, while the other group uses a minoxidil solution in the same manner. Both treatments continue for a period of 12 weeks. The results are evaluated after this period to assess the extent of hair growth improvement in each group. The study takes place in a hospital setting, ensuring that data is collected thoroughly and analyzed using statistical software, which helps in reaching reliable conclusions about the treatments' effectiveness.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.190 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Male
Biological sex of participants that are eligible to enroll.From 20 to 50 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Sheikh zayed Medical College and Hospital, Rahim Yar Khan, Punjab 644200
Rahim Yar Khan, PakistanOpen Sheikh zayed Medical College and Hospital, Rahim Yar Khan, Punjab 644200 in Google Maps