Using onion extract gel with ultrasound to improve cesarean scars
Effect of Onion Extract Nanoparticle Gel Phonophoresis on Postsurgical Scar of Cesarean Section
This study tests if a special onion extract gel used with ultrasound can help improve the healing and appearance of cesarean scars in women who are a few months post-surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | Female |
| Sponsor | October 6 University Academic / other |
| Locations | 2 sites (Cairo and 1 other locations) |
| Trial ID | NCT06658444 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of a nanoparticle gel containing onion extract applied through phonophoresis on the scars resulting from cesarean sections. The intervention aims to enhance scar healing and improve the aesthetic appearance of the scars, which can significantly affect women's quality of life. Participants will receive either the active treatment or a sham ultrasound to assess the effectiveness of the onion extract gel. The study focuses on women who are 2-3 months post-surgery and aims to provide localized treatment to reduce scar formation and associated discomfort.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18 and older who have undergone their first elective cesarean section and are experiencing postsurgical scars 2-3 months after surgery.
Not a fit: Patients with skin diseases, cognitive impairments, or those with conditions that may delay healing, such as diabetes or cardiovascular issues, may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly improve the appearance of cesarean scars and enhance the quality of life for affected women.
How similar studies have performed: Previous studies have shown promising results for the use of onion extract in improving scar appearance, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Their ages will be ≥18 years old. All women had given birth via elective abdominal transversal C-section for the first time. All women suffering from Postsurgical Scar Of Cesarean-Section about 2-3 months post-surgery. All women will provide an informed consent form agreeing to participate and publication of the study results Exclusion Criteria: Any pathological conditions or associated injuries affect the result of the study. Skin disease. Cognitive and psychological impairment. Patients have implanted electronic devices, such as cardiac pacemakers, to prevent ultrasound interference. Women with diabetes, cardiovascular problems, or a previous history of any disorder may alter sensation and delay the healing process which counteracts the study's goal.
Where this trial is running
Cairo and 1 other locations
- Heba — Cairo, Egypt (Recruiting)
- Heba — Cairo, Egypt (Recruiting)
Study contacts
- Principal investigator: Heba Haridy, doctoral — Egypt
- Study coordinator: Heba Haridy, doctoral
- Email: Heba.Ahmed.PT@o6u.edu.eg
- Phone: 01117671712
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.