Aloe Vera on Caesarean Section Wound (NCT05223127) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Aloe Vera on Caesarean Section Wound
60 participantsStarted 2024-08-01
Plain-language summary
Conducting clinical research in line with the literature recommendation, with a method that is low-cost, accessible, easy-to-use, and examined in an evidence-based design related to cesarean section wound, which negatively affects the quality of life of women in the postpartum period, constitutes the original value and our main motivation of the project.
Who can participate
Age range18 Years – 35 Years
SexFEMALE
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Inclusion Criteria:
* In the age range of 18-35,
* Primiparous,
* Gestational week 37 and above,
* Transver incision made,
* Women who volunteered to participate in the study
Exclusion Criteria:
* Body mass index not in the range of 18.5-24.9,
* Having pregnancy complications (such as preeclampsia and diabetes),
* Having chronic diseases (such as anemia, coagulopathy, cardiovascular diseases and respiratory and kidney diseases),
* Smoking or substance use,
* Those who use drugs that affect wound healing (glucocorticoids, anticoagulants, immunosuppressants, antibiotics and chemotherapy drugs before cesarean section),
* Postpartum fever (≥38 ◦C),
* Conditions that cause excessive stretching of the uterus (multiple pregnancy, polyhydramnios),
* Self or baby in need of intensive care,
* Having had a hysterectomy or myomectomy during the operation,
* The operation takes more than 90 minutes,
* Individuals who do not want to withdraw from the study