Could a chitosan gel help athletes heal hamstring injuries faster?
NCT ID NCT07544004
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether adding a gel called chitosan, applied with ultrasound (phonophoresis), to standard exercise rehab helps athletes with recurrent hamstring strains recover better. Eighty male recreational football players will either get the real treatment or a sham version. Researchers will measure pain, function, strength, flexibility, and healing using ultrasound scans.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- chitosan phonophoresis (a gel applied with ultrasound)
- What this could lead to
- If it works, this could offer a way to speed up healing and improve muscle function in athletes with recurring hamstring injuries.
- What could go wrong
- This is a small, early-stage trial with only 80 male football players, so results may not apply to everyone. The treatment is added to standard rehab, so any benefit may be modest.
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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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- 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 35 years
- Sex
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Male participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: Participants will be included in the study if they fulfill the following criteria: 1. Male recreational football players who participate in non-professional football training or matches for at least two sessions per week (each session ≥ 45 minutes) for at least the previous 12 months 2. Aged 18-35 years 3. Clinically diagnosed with a new episode of acute unilateral recurrent hamstring strain. Recurrent injury is defined as a new acute hamstring injury in the same limb and muscle group (biceps femoris, semitendinosus, or semimembranosus) as at least one previous hamstring strain that was professionally diagnosed, treated with rehabilitation, and after which the athlete returned to full participation. The previous injury must have occurred within the last 24 months 4. Current injury onset within 3-10 days of enrollment. 5. Current injury classified as Peetrons grade I or II on diagnostic musculoskeletal ultrasound performed within 7 days of enrollment by a single sonographer with at least 5 years of experience, using a 12-18 MHz linear probe in prone position (Peetrons, 2002; Heiss et al., 2025). The specific muscle involved, location within the muscle, and lesion volume (π/6 × L × W × D) will be documented at baseline 6. VISA-H score ≤ 75 at screening 7. Body mass index between 18.5 and 30.0 kg/m². 8. Able to walk independently without an assistive device. Exclusion Criteria: Participants will be excluded if they have any of the following: 1. History of hamstring tendon avulsion (complete or partial) or surgical repair in either limb. 2. Hamstring strain injury in the contralateral limb within the previous 12 months. 3. Concomitant lower extremity or lumbopelvic pathology that prevents safe completion of testing at maximal effort, including but not limited to knee ligament injury, meniscal injury, hip labral pathology, sacroiliac joint dysfunction, or lumbar disc herniation with radiculopathy. 4. Neurological disorder affecting lower extremity motor or sensory function such as peripheral neuropathy, lumbar radiculopathy, or multiple sclerosis. 5. Known allergy or hypersensitivity to chitosan, chitin, or shellfish, identified by self-report on a standardized allergy screening questionnaire at enrollment 6. Active skin disease, open wounds, or dermatitis over the posterior thigh of the affected limb. 7. Corticosteroid injection to the ipsilateral hamstring within the previous 6 months 8. Systemic conditions impairing healing such as diabetes mellitus, immunosuppressive therapy, chronic kidney disease, autoimmune connective tissue disorders, or coagulation disorders. 9. Use of pharmacological agents or supplements with known effects on tissue healing (such as growth hormone, anabolic steroids, or collagen supplements) within the previous 3 months.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Cairo Uneversity
Cairo, Egypt
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Other studies related to the condition(s) this trial covers.
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- New model aims to predict hamstring injuries before they happen
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- New study aims to kick hamstring injuries out of the game
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