Predictors of Severe Postoperative Pain Within 24 Hours After Elective Cesarean Delivery Under Spinal Anesthesia
Recruiting · NCT07789301 · Observational (researchers observe without assigning treatment)
View the official record on ClinicalTrials.gov →Interventions studied
Observational Assessment of Postoperative Pain
What this trial is about
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.
Who can take part
Age range
18 Years to 45 Years
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Pregnant women aged 18-45 years.
- Elective cesarean delivery under spinal anesthesia.
- Ability to understand Turkish.
- Written informed consent.
Exclusion criteria
- Emergency cesarean delivery.
- Conversion to general anesthesia.
- Major obstetric hemorrhage.
- Intensive care requirement.
- Chronic opioid use.
- Severe psychiatric or neurological disease.
- Inability to communicate.
Where it is running
1 location listed.
- Bursa City Hospital - Bursa, Nilüfer, Turkey (Türkiye)