The Relationship Between Preoperative Serum Asprosin Level and Postoperative Analgesic Consumption in Patients Undergoing Caesarean Section

Launched by FIRAT UNIVERSITY · Mar 4, 2024

Keywords

ClinConnect Summary

This clinical trial is studying the relationship between a substance called asprosin, found in the blood, and pain management after a Cesarean section (C-section). Researchers want to see if higher levels of asprosin before surgery are linked to increased pain during labor and more use of pain relief medications after the C-section. They believe that understanding this connection could help improve pain management for mothers undergoing this common procedure.

To be eligible for this study, participants must be pregnant women who are scheduled for an elective C-section and want to use spinal anesthesia, which is a type of pain relief during surgery. Women under 18 or those with certain health conditions—like diabetes, obesity, or serious pregnancy complications—cannot participate. If you join the study, you'll help researchers learn more about how asprosin levels affect pain, which could lead to better care for future patients.

Gender

FEMALE

Eligibility criteria

• Inclusion Criteria:
• • pregnant women who are scheduled for elective cesarean section and request spinal anesthesia for cesarean surgery,
• Exclusion Criteria:
• • Being under the age of 18
• • Having an abnormal pregnancy with preeclampsia, eclampsia, gestational diabetes, or hypertension
• • Having a comorbid desease, systemic diseases, cardiovascular disease
• • Having diabetes, obesity, or infection