Not Yet RecruitingNot Applicable

Effect of Bioptron on Scar Formation After Cesarean Section

Egypt60 participantsStarted 2025-01-27

Plain-language summary

The purpose of the study will be to determine the effect of polarized light therapy (Bioptron) on scar formation after a cesarean section.

Who can participate

Age range

20 Years – 30 Years

Sex

FEMALE

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: * The participants' ages will be ranged from 20-30 years old. * Their body mass index (BMI) will not exceed 30 kg/m2. * They will be primipara and having abdominal scar after CS. * The scar age will be extended from 6 weeks to 6 months. * All women will be medically stable when attending the study. Exclusion Criteria: * Pregnant women or women planning to become pregnant during the study period. * Women having diabetes mellitus. * Women taking immunosuppressant drugs.

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

The Patient and Observer Scar Assessment Scale (POSAS)

Timeframe: 4 weeks

Vancouver scar scale

Timeframe: 4 weeks

Trial details

NCT IDNCT06796933

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-03-18

Contact for this trial

Ghadeer Mostafa, Master

01093973398 zd94508@gmail.com

View on ClinicalTrials.gov More Cesarean Section trials