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Effect of Bioptron on Scar Formation After Cesarean Section

NCT06796933 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-01-28

No results posted yet for this study

Summary

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

Conditions

  • Cesarean Section

Interventions

OTHER

Silicon based products (silicon gel)

The participants will be treated with cosmetic creams such as Silicone-based products (silicone gels twice a day) for one month.

DEVICE

Bioptron (polarized light therapy)

The participants will be treated by polarized light therapy (Bioptron) for 15 minutes, 3 sessions per week, for one month.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Tamer Assar, Professor · Benha University

  • Mohamed Awad, Professor · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
30 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-27
Primary Completion
2025-03-18
Completion
2025-03-31

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06796933 on ClinicalTrials.gov