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Effect of Bioptron Light Therapy on Wound Healing After Caesarean Section

NCT07693478 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-07-09

No results posted yet for this study

Summary

The purpose of this study is to investigate the effect of Bioptron light therapy on wound healing after caesarean section.

Conditions

  • Cesarean Section; Complications, Wound, Dehiscence

Interventions

DRUG

Standard Postoperative Medical Care

Standard postoperative medical care consisting of analgesics, antibiotics, antiseptics, and anti-inflammatory medications prescribed by the treating obstetrician.

DEVICE

Bioptron Light Therapy

Polarized polychromatic non-coherent light therapy (480-3400 nm, energy density 2.4 J/cm², power density 40 mW/cm², 15 minutes per session, once daily for 5 consecutive days), initiated within the first 24 hours after cesarean section.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Hala Mohamed Omara, PhD · Professor, Cairo University

  • Manal Ahmed El Shafei, PhD · Assist Professor, Cairo University

  • Sameh Hussien Samir, PhD · Professor, National Research Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2026-07-12
Primary Completion
2026-08-27
Completion
2026-08-31

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 NCT07693478 on ClinicalTrials.gov