Effectiveness of Combination Therapy of Microneedling and Minoxidil in Androgenetic Alopecia of Indonesian Men
Minoxidil 5% Topical Solution
+ microneedling
Alopecia+4
+ Hair Diseases
+ Hypotrichosis
Treatment Study
Summary
Study start date: June 1, 2023
Actual date on which the first participant was enrolled.This clinical trial is focused on finding a better treatment for hair loss, specifically in Indonesian men who have androgenetic alopecia, a common form of hair loss. The study is looking at whether a combination of two treatments, microneedling and minoxidil, is more effective than just using minoxidil alone. Hair loss can affect self-esteem and confidence, so finding a more effective treatment could greatly improve the quality of life for those affected. The trial aims to see if the combination therapy leads to more hair growth and thicker hair than using only minoxidil. Participants in this trial are divided into two groups. One group uses only minoxidil, which is a topical medication applied directly to the scalp. The other group receives both microneedling, a procedure that uses tiny needles to stimulate the scalp, and minoxidil. Researchers will compare the results between these groups by measuring hair density, which refers to the number of hairs in a given area of the scalp, and hair diameter, which indicates the thickness of individual hairs. The study is designed to determine which treatment approach has the best outcomes in improving hair growth and thickness.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.36 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 18 to 59 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
ExperimentalGroup II
ExperimentalStudy 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