Actively Recruiting
Impact of Combined Intravenous-Inhalational vs Inhalational Anesthesia on QoR-15 Recovery Scores in Gynecologic Surgery
Led by Sakarya University · Updated on 2026-04-02
100
Participants Needed
1
Research Sites
78 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to compare the effects of combined intravenous-inhalational anesthesia versus inhalational anesthesia alone on postoperative recovery in patients undergoing elective gynecologic surgery. A total of 100 patients, aged 18-65 years and classified as ASA I-III, scheduled for elective gynecologic procedures at Sakarya University Faculty of Medicine Training and Research Hospital, will be included. The sample size was calculated based on the primary outcome, the Quality of Recovery-15 (QoR-15) score. Patients will complete the QoR-15 questionnaire preoperatively, before knowing which anesthesia method will be applied. Postoperative QoR-15 scores will be collected on postoperative days 1 and 2, and intraoperative data will be obtained from anesthesia records. The study evaluates postoperative recovery using QoR-15 scores, covering physical comfort, emotional state, psychological support, pain, and ability to perform daily activities. Higher scores indicate better recovery, whereas lower scores indicate impaired postoperative recovery.
CONDITIONS
Official Title
Impact of Combined Intravenous-Inhalational vs Inhalational Anesthesia on QoR-15 Recovery Scores in Gynecologic Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 to 65 years
- Scheduled for elective gynecologic surgery at Sakarya University Faculty of Medicine Training and Research Hospital
- Classified as ASA I to III
- Able to understand and complete the Quality of Recovery-15 questionnaire
- Provided written informed consent
You will not qualify if you...
- Severe comorbidities beyond ASA III
- Advanced neurological disease or cognitive impairment
- Known allergy to anesthetic drugs used in the study
- Classified as ASA IV or V
- Refusal to participate in the study
- Emergency or urgent surgery
AI-Screening
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Trial Site Locations
Total: 1 location
1
Sakarya University Training and Research Hospital
Sakarya, Turkey (Türkiye), 54290
Actively Recruiting
Research Team
M
melike kar ünlü, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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