Stromal Vascular Fraction vs Platelet Rich Plasma for Androgenetic Alopecia
stromal vascular fraction or platelet rich plasma
Alopecia+4
+ Hair Diseases
+ Hypotrichosis
Treatment Study
Summary
Study start date: August 30, 2024
Actual date on which the first participant was enrolled.This clinical trial focuses on developing effective treatments for androgenetic alopecia, commonly known as male or female pattern baldness. The study targets individuals who are experiencing hair thinning or hair loss, aiming to compare the effectiveness of two treatments: stromal vascular fraction (SVF) and platelet-rich plasma (PRP). By investigating these methods, the research seeks to provide better solutions for hair regrowth and improve overall hair density and thickness, addressing a significant concern for those suffering from this condition. Participants in the study undergo a process where their scalp is divided into two sections. One section receives an injection of SVF, which is derived from processed fat tissue, while the other section receives an injection of PRP, obtained from their own blood. The injections are given under sterile conditions with minimal discomfort, using fine needles. The effectiveness of these treatments is evaluated over a six-month period through various measures, including photographs, patient and physician assessments, and detailed hair analysis using trichoscopy. This comprehensive approach helps determine the potential benefits and improvements in hair growth and quality for the participants.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.20 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 60 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
Secondary 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