Enhanced Recovery Protocol Compliance and Quality of Recovery After Cesarean Delivery
Recruiting · NCT07790471 · Observational (researchers observe without assigning treatment) · Lead sponsor: Bursa City Hospital
View the official record on ClinicalTrials.gov →Interventions studied
Assessment of Enhanced Recovery Protocol Compliance
What this trial is about
This prospective observational study will evaluate whether adherence to enhanced recovery after cesarean delivery protocols is associated with postoperative recovery quality in women undergoing elective cesarean delivery under spinal anesthesia. A total of 150 participants will be enrolled. Recovery quality will be assessed using the Turkish version of the Obstetric Quality of Recovery-10 questionnaire at 24 hours after surgery. Pain, opioid use, nausea, mobilization, oral intake, breastfeeding, and patient satisfaction will also be evaluated.
Who can take part
Age range
18 Years and older
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Age 18 years or older
- Scheduled for elective cesarean delivery
- Planned spinal anesthesia
- American Society of Anesthesiologists physical status II or III
- Ability to read and understand Turkish
- Provision of written informed consent
Exclusion criteria
- Emergency cesarean delivery
- General anesthesia or conversion from spinal to general anesthesia
- Major obstetric hemorrhage
- Requirement for postoperative intensive care
- Chronic opioid use
- Chronic pain syndrome
- Severe psychiatric disease
- Severe neurological disease
- Inability to communicate
- Cognitive impairment preventing completion of study questionnaires
- Refusal to participate
Where it is running
1 location listed.
- Bursa City Hospital - Bursa, Nilüfer, Turkey (Türkiye)