Gynecologic Surgical Procedures

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Review clinical trials related to Gynecologic Surgical Procedures. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Intraperitoneal Infusion of Analgesic for Postoperative Pain Management

The study is a prospective, double-blinded, placebo-controlled multi-center trial to measure if postoperative pain and the amount of narcotics used are reduced by a clinically significant amount in women undergoing minimally invasive hysterectomy receiving a continuous infusion of intraperitoneal (IP) local anesthetic (LA) or a continuous infusion of LA combined with an NSAID compared with a control group who receives only 0.9% normal saline.

Participants needed: 120
Trial details
Phase: Phase 4Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Ying LiuUpdated: Apr 9, 2026Locations: 2
Eligibility criteria

Hysterectomy planned for a benign gynecologic reason (no evidence of, or concern... [+4]

Concern for malignancy [+3]

Status: Recruiting

Optical Biopsy in Gynecological Surgery

Optical biopsy is a new technology that generates a real-time, cell-based, high-resolution view and analysis of tissues. Observation is instantaneous and non-invasive. This allows reliable and fast diagnosis which facilitates decision making as well as patient management. The investigator have already conducted a feasibility study on the use of this new technology to evaluate ovarian and tubal pre-cancerous lesions in laparoscopy. In this new study, he wants to continue investigations, expand its use to other gynecological pathologies, and demonstrate the benefit of such a non-invasive technology in gynecology on the one hand in the diagnosis of lesions but also to appreciate the margins as accurately as possible surgical excision of tumors and / or endometriosis lesions. The investigator have set up a prospective monocentric descriptive study. The hypothesis is that optical biopsy by Cellvizio® allows to observe in real time microscopically tissues and to characterize them in the field of gynecological surgery

Participants needed: 80
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Hospices Civils de LyonUpdated: Jan 15, 2026Locations: 2
Eligibility criteria

Women aged 18 years or more [+6]

Interview revealing disorder entailing unacceptable risk of postoperative compli... [+8]

Status: Recruiting

Comparing CCI and POSSUM for Predicting Oncogynecologic Surgery Complications

With the global rates of gynecologic cancers on the rise, optimizing perioperative care is imperative. Accurate risk prediction is essential for enhancing patient care, directing preoperative interventions, and facilitating informed decision-making in oncology. This research compares two widely-used risk assessment tools: the Charlson Comorbidity Index (CCI) and the Physiological and Operative Severity Score for the enUmeration of Mortality and Morbidity (POSSUM), in predicting perioperative outcomes. The CCI predominantly addresses comorbidities, providing simplicity and broad applicability, while POSSUM incorporates both physiological and operative factors for a more comprehensive risk assessment. Despite their application across various surgical specialties, the specific utility of these tools in onco-gynecologic surgery remains insufficiently explored. The study aims to evaluate the effectiveness of CCI and POSSUM in predicting perioperative complications, with a focus on the incidence of these complications, length of hospital stay, and 30-day mortality. The implementation of these risk tools may enhance multidisciplinary risk management, thus improving patient outcomes in gynecologic oncology surgery.

Participants needed: 300
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Mahidol UniversityUpdated: Dec 17, 2025Locations: 1
Eligibility criteria

Age > 18 years [+1]

Patient required emergency surgery from any indication [+1]

Status: Not yet recruiting

Comparing Intra-Abdominal Pressure During Gynecologic Laparoscopy

The goal of this clinical trial is to learn if the level of intra-abdominal pressure during benign gynecologic laparoscopic surgery impacts postoperative pain. The main question it aims to answer is: • Does use of low (8 mmHg) versus standard (15 mmHg) intra-abdominal pressure impact postoperative pain? Researchers will compare the use of low (8 mmHg) versus standard (15 mmHg) intra-abdominal pressure. Participants will: * Undergo their regular scheduled gynecologic laparoscopic surgery * Complete pain measures one hour, 3 hours, and 24 hours after surgery

Participants needed: 190
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Nassau University Medical CenterUpdated: Oct 29, 2025Locations: 1
Eligibility criteria

Undergoing benign gynecologic laparoscopic surgery with eligible procedures, inc... [+6]

Participants with the following diseases will be excluded due to their diseases... [+13]