UnknownNot Applicable

Role of Local Skin Incision Infiltration by Oxytocin On Wound Healing

Egypt120 participantsStarted 2023-03-01

Plain-language summary

caesarean section rate in Egypt has reached about 60% between primgravidae. Wound complications are of the most common morbidities following cesarean section. The prevalence of wound infection and disruption after cesarean has been reported as 3-15%, averagely speaking 6% and 2-42% in various studies. These complications affect mother's quality of life due to stress, anxiety, delay in mother's ability and health recovery

Who can participate

Age range

20 Years – 35 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: * Primigravidae women, * Age group from 20- 35 years old. * Gestational age 37-41 weeks, and * Elective caesarean section due to obstetrics indication. * The patient signed an Informed Consent Form authorizing their inclusion Exclusion Criteria: * Multiparous women, * Assisted vaginal delivery, * Normal vaginal delivery, * Emergency caesarean section, * Preterm pre labour rupture of membrane, * Primiparous women with age above 35 years old, * Primiparous women with known connective tissue disease and * Women suffering from chronic diseases such as diabetes, hypertension, cardiovascular diseases, psychiatric diseases, cancer * Smoking Women

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

Wound healing after Oxytocin injecton

Timeframe: from baseline to 6 days after the Cesarean operation

Pain Relief

Timeframe: From base line to 6 hours postoperatively

Trial details

NCT IDNCT05745935

SponsorEgymedicalpedia

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2025-03-01

Contact for this trial

Assem Anour, Professor

01118996837 dramoussa77@hotmail.com

View on ClinicalTrials.gov More Wound Heal trials