Can exosome shots outperform minoxidil for baldness?
NCT ID NCT07776015
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This trial tests whether intradermal injections of exosomes—tiny particles that help cells communicate—can regrow hair in people with androgenetic alopecia (common pattern baldness) better than the standard topical minoxidil treatment. Forty participants will receive either exosome injections or minoxidil for three months, with doctors evaluating hair improvement using a global scale and safety monitoring. The goal is to see if this novel approach offers a more effective or convenient alternative for hair loss.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Intradermal injections of exosomes (Exomide) compared with 5% topical minoxidil solution
- What this could lead to
- If exosome injections prove effective, they could offer a new, non-surgical option for treating common pattern hair loss, potentially with better results than standard topical treatments.
- What could go wrong
- This is a small, early-stage trial with only 40 participants, so results may not apply broadly. Exosome injections carry risks like injection-site reactions, and their long-term safety and effectiveness are not yet established.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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40 people
The number who actually took part.
- Started
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Apr 2023
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 55 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Were male or female patients with a confirmed diagnosis of androgenetic alopecia (AGA). Had not received any treatment for AGA for at least 6 months before study initiation. Provided written informed consent. Agreed to attend the scheduled follow-up assessments and undergo photographic documentation. Exclusion Criteria: * Concurrent scalp diseases. A history of bleeding disorders. Current use of anticoagulant medications. Known keloidal tendency. History of psoriasis or lichen planus. Significant cardiac, hepatic, or renal disease. Any major systemic illness. Pregnancy or lactation.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Tanta University Hospitals
Tanta, Egypt
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Other studies related to the condition(s) this trial covers.
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