CompletedNot Applicable

Combined LASERs and PRP for Postacne Scars

Italy, Kuwait32 participantsStarted 2018-10-01

Plain-language summary

This study evaluates a new combined technique using two different laser wavelengths and Platelets Rich Plasma (PRP) to treat post-atrophic acne scars. Within the available knowledge of laser-tissue interactions and effects of PRP on wound healing, we will explore the clinical effects of our new combination procedure on a histopathological and immunohistochemical basis for guiding future post acne scars clinical research.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Patients with atrophic post-acne scars.
. Patients without surgical \&/or LASER resurfacing treatment for acne scars within the last 6 months.

Exclusion criteria

. Pregnancy
. Present or past history of hypertrophic scars or keloids
. Present or past history of photosensitivity dermatoses including Connective Tissue Diseases.
. Present history of herpes infection
. Present history of Anemia (HGB \< 10 g/dl), Thrombocytopenia \&/or Platelets dysfunction.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Change in Patients' response denoting early Clinical improvement

Timeframe: 4 weeks after the 1st session

Final Clinical improvement assessed using (0-10) scoring scale by blind assessors

Timeframe: 12 weeks after the 4th session

Trial details

NCT IDNCT03809416

SponsorDEKA S.r.l.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2019-06-30

View on ClinicalTrials.gov More Atrophic Acne Scar trials