Actively Recruiting
St. John's Wort Oil for Wound Healing and Pain After Cesarean Section
Led by Sakarya University · Updated on 2025-06-10
80
Participants Needed
1
Research Sites
44 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Cesarean section refers to the surgical procedure in which the fetus is delivered via an incision, typically performed when vaginal delivery is not possible due to high-risk conditions. In recent years, the rate of cesarean deliveries has increased significantly. The quality of treatment and care is crucial in ensuring proper surgical wound healing following cesarean birth. Various new methods and products have been developed for wound healing and care in recent years, some of which are derived from herbal sources. The limitations of pharmacological methods used in the postpartum period, such as treatment failure, concerns about potential harm to the mother and infant, adverse side effects, negative impact on breastfeeding, emergence of resistant microorganisms, and ineffectiveness of current antibiotics, have led individuals to seek alternative natural remedies. Hypericum perforatum (commonly known as St. John's Wort) is frequently used in the postpartum period due to its antimicrobial and antioxidant properties. This study aims to examine the effects of Hypericum perforatum on wound healing and pain in women following cesarean delivery.
CONDITIONS
Official Title
St. John's Wort Oil for Wound Healing and Pain After Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Volunteering to participate in the research
- Having had a cesarean section
- Her first cesarean section
- Being fluent in Turkish
You will not qualify if you...
- Not wanting to participate in the research
- The existence of a communication barrier
AI-Screening
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Trial Site Locations
Total: 1 location
1
Sakarya Üniversity
Sakarya, Turkey (Türkiye), 54000
Actively Recruiting
Research Team
B
Bilge Nur Yıldırım Bayraktar Dr., PhD
CONTACT
G
Güleser ADA Dr, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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