Can threads or plasma smooth out old scars?
NCT ID NCT07775092
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This trial compares two procedures for treating post-traumatic atrophic scars (depressed scars from injury or acne). One group receives a single session of subcision (breaking up scar tissue) plus insertion of poly-L-lactic acid (PLLA) threads, while the other gets subcision combined with platelet-rich plasma (PRP) injections monthly for four months. Researchers will measure clinical improvement, patient satisfaction, side effects, and tissue changes over three months to see which approach works better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Poly-L-lactic acid (PLLA) threads or platelet-rich plasma (PRP), both combined with subcision
- What this could lead to
- If effective, this could offer a better, longer-lasting option for improving the appearance of post-traumatic atrophic scars.
- What could go wrong
- This is a small, early-stage comparative study with a short follow-up. Results may not generalize, and both procedures carry risks like infection or scarring.
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
-
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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48 people
The number who actually took part.
- Started
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Feb 2023
- Finished
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Aug 2024
- 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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16 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: * Patients with post-traumatic atrophic scars. Scar duration of at least 1 year. No treatment received during the previous 6 months. Exclusion Criteria: * Keloids Immunosuppression Coagulative disorders Thrombophilic disorders Any chronic diseases
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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
-
Tanta University Hospitals
Tanta, Egypt
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