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Exosome Effect on Prevention of Hairloss

Placental Mesenchymal Stem Cells-derived Exosome for Hairloss

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05658094
Enrollment
20
Registered
2022-12-20
Start date
2022-08-01
Completion date
2023-10-29
Last updated
2022-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hair Loss, Alopecia

Keywords

Exosome

Brief summary

Many people suffer from alopecia, which is caused by hereditary factors, emotional stress, and psychiatric disorders. There are devastating physical and psychological consequences as a result. Exosomes are isolated from donated human amniotic mesenchymal stem cells and purified using specific processing. Exosomes are unique in that they are derived from stem cells and contain a wide range of growth factors. The latest generation of natural products for treating hair loss is exosomes.

Detailed description

Exosomes contain a variety of growth factors that are derived from stem cells. As they are so small, they can be hidden in the bloodstream and carry different types of proteins. The Wnt-β-catenin pathway is thought to play a major role in the pathogenesis of hair loss. The only FDA-approved medications for the treatment of hair loss are minoxidil (a vasodilator) and finasteride (a selective inhibitor of 5α reductase type II and III isoforms). However, these drugs have not been very perfect. Both have been associated with limited efficacy, duration of effect, and several significant side effects. Regenerative medicine using cell products is looking for a way to heal faster and less cost. Present research focus on Exosome efficacy on hairloss.

Interventions

DEVICEExosome

Each patients will receive 4 injection with an interval of 14 days during two months

Sponsors

Isfahan University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

subjects able to read the documents and have medical coverage Subjects have a hair loss grade as below criteria: 1. BASP grade: Basic type (M2 to M3, or C2 to C3, or U1 to U3) or Specific type (V1 to V3, or F1 to F3) 2. For female: Ludwig grade: Ⅰ to Ⅱ 3. For male: Norwood-Hamilton grade: III to IV 4. Hair density by phototrichogram: 60 to 190 hair/cm2 5. Telogen hair ≥ 5% Subject agreeing not to apply any topical treatment Subject agreeing to use a neutral shampoo

Exclusion criteria

1. Sick subject in situation of emergency. 2. Subjects who have hereditary history of hairloss 3. Pregnant Females 4. Subject using topic cosmetic treatment or oral nutritional supplement likely to interfere on hair loss parameters during the last 3 months prior to the start of the study (screening) 5. Subjects who have a medical treatment for alopecia or having stopped it from than 3 months

Design outcomes

Primary

MeasureTime frameDescription
Change in mean total hair density (hair/cm2)0 monthsMeasurement of hair density by phototrichogram: change in mean total hair density (hair/cm\^2)
visual assessment before and after6 monthsVisual Assessment using the clinical picture by a general physician

Secondary

MeasureTime frameDescription
Change in mean Telogen and Anagen hair density0, monthsMeasurement of telogen and Anagen hair density before and after trial

Countries

Iran

Contacts

Primary Contactleila dehghani, Dr
l_dehghani2002@yahoo.com+393517261300

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026