About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
In the age range of 18-35,
Primiparous,
Gestational week 37 and above,
Transver incision made,
Disqualifiers
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,
Trial design
Parallel
Treatments tested in this trial
Aloe vera
Other interventionThe leaves of Aloe vera (Aloe barbadensis) will be identified and verified by Selçuk University Faculty of Agriculture. Aloe vera leaves will be washed with antiseptic solution and cut crosswise using gloves and sterile knife. The thick epidermis will be removed from the middle of the leaf. The gel will be obtained from the parenchyma of the thick juicy leaves of aloe vera.
Treatment groups
Trial outcomes
Primary outcomes
Wound healing
It will be assessed using the REEDA scale.
Secondary outcomes
Ache
It will be assessed using the McGill Pain Scale Short Form.
Life quality
It will be assessed using the SF-36 Quality of Life Scale.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: