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Recruiting NCT07204795

NCT07204795 Effect of Preoperative Oral Carbohydrate Drink on ObsQoR-10 Score After Elective Cesarean Under Neuraxial Anesthesia

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Clinical Trial Summary
NCT ID NCT07204795
Status Recruiting
Phase
Sponsor Ataturk University
Condition ObsQor-10
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2025-05-20
Primary Completion 2026-04

Trial Parameters

Condition ObsQor-10
Sponsor Ataturk University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 100
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2025-05-20
Completion 2026-04
Interventions
Distilled water groupCarbohydrate Drink

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Brief Summary

The goal of this clinical trial is to determine whether a preoperative oral carbohydrate-rich clear drink can improve recovery in women undergoing elective cesarean section under neuraxial anesthesia. The main outcomes it aims to answer are: Primary Outcome: Does the carbohydrate drink improve ObsQoR-10 scores at 24 and 48 hours postoperatively? Secondary Outcomes: Does it reduce patients' hunger, thirst, and anxiety levels? Researchers will compare patients receiving a 400 ml oral carbohydrate-rich clear drink 2 hours before surgery (Group A) to those receiving 400 ml distilled water (Group B), to assess differences in recovery and comfort. Participants will: Be randomized into two equal groups (n=50 each) using a computer-generated randomization table Receive standardized anesthesia and postoperative analgesia

Eligibility Criteria

Inclusion Criteria: Age ≥18 years Scheduled for elective cesarean section under neuraxial anesthesia Gestational age ≥37 weeks Exclusion Criteria: Contraindication to neuraxial anesthesia Age \<18 years Refusal to participate in the study Obesity Hiatal hernia Intestinal obstruction Gastroesophageal reflux disease (GERD) Diabetes mellitus Fetal anomalies Eclampsia or preeclampsia Substance abuse Chronic pain conditions

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