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Clinical Research Directory

Browse clinical research sites, groups, and studies.

6 clinical studies listed.

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Gynecologic Surgery

Tundra lists 6 Gynecologic Surgery clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07506798

Impact of Combined Intravenous-Inhalational vs Inhalational Anesthesia on QoR-15 Recovery Scores in Gynecologic Surgery

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.

Gender: All

Ages: 18 Years - 65 Years

Updated: 2026-04-02

Gynecologic Surgery
Postoperative Recovery
Anesthesia
NOT YET RECRUITING

NCT07251101

Hemodynamic Effects of Remimazolam vs Propofol During Robot-assisted Gynecologic Surgery

This single-center study at CHA Ilsan Medical Center compares intraoperative hemodynamics between remimazolam- and propofol-based total intravenous anesthesia (TIVA) in patients undergoing robot-assisted gynecologic surgery requiring pneumoperitoneum and steep Trendelenburg positioning.

Gender: FEMALE

Ages: Any - 65 Years

Updated: 2026-03-27

1 state

Anesthesia, Intravenous
Hemodynamic Stability
Gynecologic Surgery
ACTIVE NOT RECRUITING

NCT05071976

A Study of Near-Infrared Fluorescence Imaging With ICG During Reconstructive Gynecologic Surgery

The objective of this study is to assess whether Near-Infrared Fluorescence/NIR Imaging perfusion alters intraoperative management of the flap or of the participant wound bed.

Gender: FEMALE

Ages: 18 Years - Any

Updated: 2025-10-31

2 states

Gynecologic Surgery
NOT YET RECRUITING

NCT07146178

Long-term Follow-up of Bio-signals and Quality of Recovery Following Implementation of ERAS

The goal of this clinical trial is to evaluate the effect of an Enhanced Recovery After Surgery(ERAS) protocol in patients undergoing gynecologic laparoscopic surgery under general anesthesia. The main question it aims to answer is: Does the ERAS protocol improve the quality of recovery compared to standard treatments? Researchers will compare ERAS protocol with standard treatment to see if ERAS protocol improves the quality of recovery after surgery. Participants will: * Receive ERAS protocol during the hospitalization * Undergo bio-signal monitoring for one month using Hi-Cardi Plus device and Galaxy Watch 7 * Visit the hospital at one week and one month after discharge * Complete questionnaires(QOR-15K, WHO-DAS 2.0, EQ-5D-3L) at 24 hours after surgery, at discharge, one week after discharge, and one month after discharge

Gender: FEMALE

Ages: 20 Years - 70 Years

Updated: 2025-08-28

1 state

Gynecologic Surgery
General Anesthesia
ACTIVE NOT RECRUITING

NCT07114965

Effects Of Quadratus Lumborum Type 1 Block And Transversalis Facial Plane Block On Acute Pain In Gynecological Surgery

This study was conducted to evaluate the effectiveness of Quadratus Lumborum Type 1 and Transversalis Fascial Plane blocks on postoperative acute pain in gynecology operations.

Gender: FEMALE

Ages: 18 Years - 80 Years

Updated: 2025-08-11

Postoperative Pain
Gynecologic Surgery
RECRUITING

NCT05526534

A RCT on the Preventive Effect of HFNC on Postoperative Pulmonary Complications in Patients With Gynecologic Neoplasms

Patients at high risk of post-operative pulmonary complications (PPC) will be screened out from gynecological tumor patients undergoing surgical treatment, and randomly assigned into the HFNC group and control group, which uses conventional nasal cannula oxygen therapy. The primary outcome is the incidence of PPC, including postoperative hypoxemia, atelectasis, pneumonia, etc. Secondary outcomes are the improvement of postoperative oxygenation, antibiotic use, length of hospital stay, adverse events related to oxygen therapy, etc.

Gender: FEMALE

Ages: 18 Years - 90 Years

Updated: 2025-05-23

1 state

Gynecologic Surgery
High-flow Nasal Cannula
Post-operative Pulmonary Complications