Combined IV plus inhaled anesthesia versus inhaled anesthesia alone for recovery after gynecologic surgery
Effects of Combined Intravenous-Inhalational Anesthesia Versus Inhalational Anesthesia on Postoperative Recovery in Gynecological Operations: A Comparison Based on QoR-15 Scores
NA · Sakarya University · NCT07506798
This test will see if adding intravenous anesthesia to inhaled anesthesia helps adults aged 18–65 recover better after elective gynecologic surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Sakarya University (other) |
| Locations | 1 site (Sakarya) |
| Trial ID | NCT07506798 on ClinicalTrials.gov |
What this trial studies
One hundred adults (ages 18–65) classified ASA I–III undergoing elective gynecologic procedures at Sakarya University Training and Research Hospital will receive either combined intravenous-inhalational anesthesia or inhalational anesthesia alone. Patients will complete the QoR-15 questionnaire before surgery and again on postoperative days 1 and 2, while intraoperative data will be collected from anesthesia records. The primary outcome is the QoR-15 recovery score, which covers physical comfort, pain, emotional state, psychological support, and ability to perform daily activities. The trial compares postoperative recovery quality between the two anesthesia approaches.
Who should consider this trial
Good fit: Adults aged 18–65 with ASA I–III undergoing elective gynecologic surgery at Sakarya University who can provide informed consent and complete the QoR-15 are eligible.
Not a fit: Patients with severe comorbidities beyond ASA III, advanced neurological/cognitive impairment, emergency surgeries, or known allergies to the anesthetic drugs used are unlikely to benefit or be eligible.
Why it matters
Potential benefit: If successful, the combined anesthesia approach could improve immediate postoperative comfort and faster return to daily activities after gynecologic surgery.
How similar studies have performed: Prior comparisons of combined intravenous-inhalational versus inhalational anesthesia have shown mixed results, with some studies reporting modest improvements in recovery metrics but no consistent superiority.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients aged 18-65 years 2. Scheduled for elective gynecologic surgery at Sakarya University Faculty of Medicine Training and Research Hospital 3. Classified as ASA I-III 4. Able to understand and complete the QoR-15 questionnaire 5. Provided written informed consent Exclusion Criteria: 1. Severe comorbidities (beyond ASA III) 2. Patients with advanced neurological disease or cognitive impairment 3. Known allergy to anesthetic drugs used in the study 4. Classified as ASA IV-V 5. Refusal to participate in the study 6. Emergency or urgent surgery
Where this trial is running
Sakarya
- Sakarya University Training and Research Hospital — Sakarya, Turkey (Türkiye) (RECRUITING)
Study contacts
- Study coordinator: melike kar ünlü, MD
- Email: Melikekar2015@gmail.com
- Phone: 905079790381
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Gynecologic Surgery, Postoperative Recovery, Anesthesia