RecruitingNCT07789301

Predictors of Severe Postoperative Pain Within 24 Hours After Elective Cesarean Delivery Under Spinal Anesthesia

Predictors of Severe Postoperative Pain Within the First 24 Hours After Elective Cesarean Delivery Under Spinal Anesthesia: A Prospective Observational Study


Sponsor

Bursa City Hospital

Enrollment

200 participants

Start Date

Jul 15, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

This prospective observational study aims to identify predictors of severe postoperative pain during the first 24 hours after elective cesarean delivery under spinal anesthesia. Preoperative, intraoperative, and postoperative factors will be evaluated to determine their association with severe postoperative pain.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Observational Assessment of Postoperative Pain for people with acute pain, cesarean section, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 45 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERObservational Assessment of Postoperative Pain

Participants will receive routine spinal anesthesia and standard perioperative care for elective cesarean delivery. Preoperative, intraoperative, and postoperative variables will be recorded without any study-specific intervention.


Locations(1)

Bursa City Hospital

Bursa, Nilüfer, Turkey (Türkiye)

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NCT07789301


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