The Effectiveness of Allogenic Mesenchymal Stem Cells Therapy on Hair Regrowth in Androgenetic Alopecia.

NCT ID: NCT06764329

Last Updated: 2025-01-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

PHASE1/PHASE2

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-12-25

Study Completion Date

2025-08-30

Brief Summary

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The goal of this study is to learn if mesenchymal stem cell therapy (treatment group) can effectively treat adrogenic alopecia or male-pattern baldness, when compared to normal saline (given to placebo group). It will also assess the differences in patient satisfaction. The main focus will be to:

1. Compare the average hair regenerative effect of mesenchymal stem cells versus Placebo, in treatment of androgenetic alopecia.
2. To determine and compare the investigators assessment and patient satisfaction in both groups.

Patients in treatment group will receive single session of MSC therapy injected in the scalp and placebo group will receive 0.9% saline solution. The participants will be followed for 12 weeks. The hair density and thickness will be mesured along with clinicians assessment and participant's satisfaction level.

Detailed Description

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1. Introduction:

Androgenetic Alopecia (AGA) is a common form of hair loss affecting both men and women, characterized by the miniaturization of hair follicles due to the influence of a variety of factors including androgens and genetics. AGA affects a sizeable portion of the population worldwide, affecting males and females both.1 While many accept it as a normal physiological process of ageing, for others it causes remarkable concern and worry, especially pertaining to personal appearance and self-confidence. So much so leading to body image issues and even psychological disorders1,2,3. Hence it becomes empirical to treat this condition with aim to achieve patient satisfaction. Current treatment options, such as minoxidil and finasteride, have limitations in efficacy and number of adverse effects which limit their use.1 Mesenchymal derived stem cells (MSCs) have emerged as a potential therapeutic option due to their regenerative and immunomodulatory properties.1 Cell-based therapy has seen a significant rise as an alternative for treating medical disorders in recent years. Specifically, stem cell therapy has been applied to address various dermatological conditions, including alopecia. Stem cells (SCs) are known to play a crucial role in initiating the hair growth cycle and remodeling.1 Emerging evidence suggests that stem cells may be responsible for releasing cytokines, chemokines, and specific growth factors like bFGF, VEGF, IGF-1, HGF, and TGF-β1. These molecules initiate cell repair processes through angiogenesis, immunomodulation, cell differentiation, and proliferation. In the scalp, they exert a paracrine effect on neighboring cells and tissues, promoting hair follicle growth, adjusting hair growth patterns, regulating follicle size via angiogenesis, and supporting the retention of the anagen phase.2,3 A RCT comparing Adipose derived Stem Cell Constituent Extract (ADSC-CE) with Placebo (Distilled water), carried out at Busan National University Yangsan Hospital, Korea showed significant statistical improvement in mean hair count and mean hair diameter in Intervention Group (IG) versus Control Group (CG) 16 weeks post treatment. Change from baseline in Hair Diameter was 0.008 ± 0.007 in IG versus 0.004 ± 0.004 in CG with p value of .023. Change from baseline in Hair counts was 3.89 ± 3.01 in IG versus 1.44 ± 1.97 in CG with p value of .025. In investigator assessment using photographs, intervention failed to show a statistically significant improvement in both groups. In the participants self-assessments, no significant intergroup differences were observed.3 Based on above evidence, there is a vast avenue of research in potential role of MSCs therapy in AGA, as an emerging approach.1,2,3 This study has the potential to pave the way for further advancements in regenerative medicine. This study aims to evaluate the efficacy and safety of MSCs in the treatment of AGA through a double-blind randomized controlled trial (RCT).

As current treatments offer limited success, this study is directed to explore potential for a novel, minimally invasive alternative with long term effectiveness and improved outcomes in hair loss management, especially in our population, addressing an unmet clinical need.
2. OBJECTIVE i. To compare the mean hair regenerative effect of Mesenchymal derived stem cells (MSCs) versus Placebo, in treatment of androgenetic alopecia (AGA).

ii. To determine and compare the investigators assessment and patient satisfaction in both groups.

Conditions

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Androgenetic Alopecia Androgenetic Alopecia (AGA)

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Double-Blind, Randomized, Placebo-Controlled Trial
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Treatment

MSC therapy group

Group Type EXPERIMENTAL

Mesenchymal Stem Cells

Intervention Type BIOLOGICAL

allogeneic bone marrow-derived mesenchymal stem cells therapy

Placebo group

Placebo (0.9% saline)

Group Type PLACEBO_COMPARATOR

0.9 % saline

Intervention Type OTHER

0.9% Saline as placebo

Interventions

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Mesenchymal Stem Cells

allogeneic bone marrow-derived mesenchymal stem cells therapy

Intervention Type BIOLOGICAL

0.9 % saline

0.9% Saline as placebo

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Male patients with AGA between age 25 to 59 years of age
* Clinical presentation consistent with Hamilton Norwood criteria grade ll to Vl
* Not currently receiving antiandrogens or minoxidil therapy.

Exclusion Criteria

* Patients with hair loss other than AGA
* Patients receiving 5-alpha reductase inhibitor or minoxidil therapy
* Patients who received PRP for at least 6 months prior to enrollment
* History of hypertrophic scars or bleeding disorders
* History of treatment with hyper or hypothyroidism
Minimum Eligible Age

20 Years

Maximum Eligible Age

59 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Pak Emirates Military Hospital

OTHER

Sponsor Role collaborator

National Institute of Blood and Marrow Transplant (NIBMT), Pakistan

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Department of dermatology, Pak-Emirates Military Hospital

Rawalpindi, , Pakistan

Site Status

National Institute of Blood and Marrow Transplant (NIBMT)

Rawalpindi, , Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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AFBMTC-2024-MSC in Alopecia

Identifier Type: -

Identifier Source: org_study_id

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