Evaluation of Mitochondrial Enzyme Activity in Cesarean Section Patients

Launched by SANLIURFA MEHMET AKIF INAN EDUCATION AND RESEARCH HOSPITAL · Jan 12, 2024

Keywords

ClinConnect Summary

This clinical trial is looking to understand how certain biochemical factors, like trace elements and specific enzymes, change in women who have a cesarean section with spinal anesthesia. The researchers want to find out how these factors affect the body during and after the surgery. To do this, they will take a small blood sample (about 10 ml) from participants before and after their surgery to compare the results.

To participate in this study, women aged 18 to 40 who are scheduled for a planned cesarean section may be eligible, as long as they are in good health (classified as ASA 1-2, which means they have no serious health issues). However, women who have certain health conditions, are older than 40, or who are having an emergency cesarean section will not be able to join. If you qualify and choose to participate, you'll simply provide a blood sample to help researchers learn more about your body's response to the surgery. This study aims to improve our understanding of how cesarean sections affect women’s health.

Gender

FEMALE

Eligibility criteria

• Inclusion Criteria:
• • 1. Patients who will undergo planned cesarean section between the ages of 18 and 40
• • 2. ASA 1-2 Patients
• Exclusion Criteria:
• • 1. Patients who refuse to participate in the study
• • 2. Patients over 40 years of age
• • 3. ASA 3-4 Patients
• • 4. Patients who underwent emergency cesarean section
• • 5. Those with known liver and kidney diseases, patients diagnosed with Diabetes Mellitus
• • 6. Pregnant women diagnosed with an abnormal baby
• • 7. Patients diagnosed with preeclampsia
• • 8. Patients with body mass index ≥ 30
• • 9. Patients who do not accept spinal anesthesia or have contraindications to the application -