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Hysterectomy clinical trials

View clinical trials related to Hysterectomy.

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NCT ID: NCT03101098 Suspended - Hysterectomy Clinical Trials

Retroperitoneal Ligation of Uterine Artery in Total Laparoscopic Hysterectomy for Enlarged Uterus

Start date: April 10, 2017
Phase: N/A
Study type: Interventional

This randomized trial is aimed to investigate the role of retroperitoneal TLH in enlarge uterus.

NCT ID: NCT03006237 Completed - Surgery Clinical Trials

IS-001 Injection Phase-1 Safety, Tolerance and Pharmacokinetics

Start date: December 2016
Phase: Phase 1
Study type: Interventional

A Phase 1 Open Label Single Center Safety, Tolerability and Pharmacokinetic Study of IS-001

NCT ID: NCT02998658 Not yet recruiting - Hysterectomy Clinical Trials

Barbed Versus Conventional Sutures for Vaginal Cuff Closure During Total Laparoscopic Hysterectomy

Start date: February 2017
Phase: Phase 2
Study type: Interventional

The aim of this study is to estimate whether the use of the barbed suture facilitates laparoscopic suturing of the vaginal cuff during total laparoscopic hysterectomy.

NCT ID: NCT02911831 Completed - Hysterectomy Clinical Trials

IV Tranexamic Acid Prior to Hysterectomy

Start date: November 2016
Phase: Early Phase 1
Study type: Interventional

The objective of this study is to determine the effect of 1g of IV tranexamic acid given within 1 hour pre-operatively on intraoperative blood loss at time of hysterectomy.

NCT ID: NCT02751073 Completed - Clinical trials for Pelvic Organ Prolapse

Evaluation of the Relationship Between Vaginal and Lower Urinary Tract Microbiomes and Infection After Hysterectomy

Start date: February 2016
Phase:
Study type: Observational

The purpose of this study is to learn more about the microbes (bacteria) that live in the vagina and the bladder. The investigators are doing this research study to understand the relationship between microbes (the microbiome) and the occurrence of urinary tract infection following surgical removal of the uterus and pelvic organ prolapse repair. The investigators expect Lactobacillus and Gardnerella will be the dominant organisms for most women. Non-Lactobacillus dominant microbiome communities will be more common in women who ultimately develop postoperative urinary tract infection.

NCT ID: NCT02741531 Completed - Hysterectomy Clinical Trials

The Effect of Partial Bladder Filling on Post-operative Time to Void in Minimally Invasive Gynecologic Procedures

Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if partially filling the bladder after laparoscopic/robotic gynecologic surgery (for benign disease) shortens the time required to spontaneously void for patients to determine if this subsequently shortens patient stay times in the Post Anesthesia Care Unit (PACU) following surgery. This intervention would be compared to the current standard of care, which involves removing the patient's Foley catheter with an empty bladder and then giving the patient up to 6 hours to void in the PACU.

NCT ID: NCT02669537 Withdrawn - Hysterectomy Clinical Trials

Utility of the GoPro Hero 3 Camera as an Educational Tool For Vaginal Surgical Skills

Start date: May 2016
Phase: N/A
Study type: Interventional

Utilization of the GoPro camera to facilitate vaginal surgical education among residents and medical students

NCT ID: NCT02621710 Completed - Clinical trials for Patient Satisfaction

Goal Achievement and Patient Satisfaction in Benign Hysterectomy

Start date: December 2015
Phase: N/A
Study type: Observational

This study evaluates patient goal achievement and satisfaction in benign hysterectomy. Patient's will state their goals prior to undergoing benign hysterectomy, and will receive a follow-up questionnaire 3 months post-operatively evaluating their perception of goal achievement and overall satisfaction. Goal achievement and satisfaction will be evaluated for association with surgical indication, surgical approach (minimally invasive vs abdominal surgery), and demographic information.

NCT ID: NCT02532361 Completed - Hysterectomy Clinical Trials

Proportion of Hysterectomy After Female Sterilization

Start date: August 2015
Phase: N/A
Study type: Observational

The objective of this study is to describe the proportion of hysterectomy in patients that had undergone sterilization through hysteroscopic device placement and the patients that had undergone sterilization through tubal ligation.

NCT ID: NCT02496130 Completed - Hysterectomy Clinical Trials

Perioperative Outcomes of Common Methods of Minimally Invasive Contained Tissue Extraction

Start date: April 2016
Phase:
Study type: Observational

The goal of this study is to compare common methods of tissue extraction at the time of minimally invasive surgery.