Clinical Trials Logo

Laparoscopic Hysterectomy clinical trials

View clinical trials related to Laparoscopic Hysterectomy.

Filter by:

NCT ID: NCT06050161 Not yet recruiting - Clinical trials for Pelvic Organ Prolapse

Evaluating Artisential Laparoscopic Instruments in Gynecologic Surgery

MIGS-ART
Start date: September 20, 2023
Phase: N/A
Study type: Interventional

This study evaluates the efficacy and safety of Artisential laparoscopic instruments in minimally invasive gynecologic surgery.

NCT ID: NCT05826119 Recruiting - General Anesthesia Clinical Trials

Intravenous Administration of Magnesium Sulfate in Laparoscopic Hysterectomy Cases

MgSO4
Start date: January 20, 2024
Phase: N/A
Study type: Interventional

In our study, it was aimed to show the contribution of intraoperative intravenous magnesium sulfate administration to peroperative opioid consumption and postoperative analgesia.

NCT ID: NCT05690087 Completed - Lidocaine Clinical Trials

Lidocaine Infusion on Optic Nerve Sheath Diameter in Laparoscopic Hysterectomy in Trendelenburg Position

Start date: February 1, 2023
Phase: N/A
Study type: Interventional

We hypothesize that intravenous lidocaine infusion may have beneficial effect to patients undergoing laparoscopic surgeries in Trendelenburg position by preventing ICP elevation.

NCT ID: NCT05645809 Recruiting - Clinical trials for Laparoscopic Hysterectomy

Clinical Trial to Evaluate the Safety and Efficacy of MONOFIX® PGCL Suture in Laparoscopic Surgery

Start date: November 3, 2022
Phase: N/A
Study type: Interventional

Clinical Trial to Evaluate the Safety and Efficacy of MONOFIX® PGCL Suture Compared to Quill MonodermTM Suture in Laparoscopic Surgery

NCT ID: NCT05570916 Recruiting - Clinical trials for Laparoscopic Hysterectomy

Zip-Stitch® in Minimally-Invasive Surgery (ZIMS) - Safety & Efficacy in Hysterectomy

ZIMS
Start date: August 17, 2023
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the safety and efficacy of the Zip-stitch® Vaginal Cuff Closure System. This will be primarily done by measuring the frequency of implant passing following system use. Also assessed will be relevant safety and efficacy endpoints as compared to a two-to-one reference group.

NCT ID: NCT04972682 Completed - Endometrial Cancer Clinical Trials

[SENTRY] Tailoring Postoperative Management Through Sentinel Lymph Node Biopsy in Low- and Intermediate-Risk Endometrial Cancer

SENTRY
Start date: July 1, 2021
Phase: N/A
Study type: Interventional

While total hysterectomy without lymph node staging is standard for low- and intermediate-risk endometrial cancer, certain histopathologic factors can necessitate additional interventions. Our study assesses the influence of sentinel lymph node (SLN) biopsy on postoperative decision-making.

NCT ID: NCT04725981 Terminated - Vaginal Infection Clinical Trials

Vaginal Stump Infection After Laparoscopic Hysterectomy

CoToIn
Start date: August 23, 2018
Phase: N/A
Study type: Interventional

Comparing two surgical techniques in relation to vaginal stump infection, analysis of patient-based and therapy-based risk factors.

NCT ID: NCT04366375 Completed - Clinical trials for Laparoscopic Hysterectomy

Pentraxin-3 in Hysterectomy Patients

Start date: January 13, 2015
Phase:
Study type: Observational

Comparison of the Tissue Trauma Markers Following Total Laparoscopic Hysterectomy vs Total Abdominal Hysterectomy

NCT ID: NCT04239547 Completed - Clinical trials for Laparoscopic Hysterectomy

Effects of Recruitment Maneuver During Intraoperative Period

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to observe the effect of respiratory recruitment maneuver on intraoperative ventilatory parameters and postoperative pulmonary complications in patients over 18 years scheduled for laparoscopic hysterectomy.

NCT ID: NCT04081727 Terminated - Clinical trials for Laparoscopic Hysterectomy

Zip-Stitchâ„¢ for Vaginal Cuff Closure in Laparoscopic Hysterectomy - Safety & Efficacy Study

Start date: November 6, 2019
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the safety and efficacy of the Zip-stitchâ„¢ Vaginal Cuff Closure System. This will be primarily done by measuring the frequency of implant passing following system use. Also assessed will be relevant safety and efficacy endpoints as compared to a two-to-one reference group (V-LOC barbed suture).