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Myomectomy clinical trials

View clinical trials related to Myomectomy.

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NCT ID: NCT03892668 Completed - Myomectomy Clinical Trials

Intravenous Oxytocin Versus Tranexamic Acid in Reducing Blood Loss During Abdominal Myomectomy.

Start date: April 30, 2019
Phase: Phase 4
Study type: Interventional

Uterine leiomyomas (fibroids) are the most common benign tumors among women. Fibroids are found in approximately 20% of women over 35 years of age. In 20-50% of patients, fibroids may cause problems such as heavy menstrual bleeding, anemia, pelvic pain, pressure symptoms from extrinsic compression of the colorectal and urinary tract. Surgery is indicated for symptomatic uterine leiomyomas; hysterectomy for women who have completed childbearing (women > 40 years old), and myomectomy for women <40 years old who wish to preserve uterus and fertility.

NCT ID: NCT03634306 Completed - Pain Clinical Trials

Ultravision Visual Clearing System in Laparoscopic Hysterectomy and Myomectomy

Start date: October 11, 2018
Phase: N/A
Study type: Interventional

This is a prospective blinded, randomized controlled study. The study will include three study arms: Patients undergoing laparoscopic hysterectomies will be randomized to one of either "Ultravision" (study arm 1) or "no Ultravision" (study arm 2, i.e. the current standard of care) groups. The study will be conducted blinded to the investigator during the procedure through patient discharge. The Ultravision system will be present in both, with the generator covered (not seen by user) and either on or off depending on the randomization. 30 patients will be enrolled, 15 per group. Five patients undergoing myomectomy will have their procedures conducted using the Ultravision (study Arm 3). Ultravision is cleared for use in all laparoscopic surgery i.e. including laparoscopic hysterectomy and myomectomy, in the United States. However, the clinical benefits arising from its use in gynecology have not yet been quantitatively assessed and published in an independent medical journal. Study Purpose: There are three main study objectives 1. To evaluate the impact of use of Ultravision device during laparoscopic hysterectomy and myomectomy on the quality of visualization in the laparoscopic field 2. To evaluate the impact of use of Ultravision device during laparoscopic hysterectomy and myomectomy on procedural characteristics 3. To evaluate the impact of use of Ultravision device during laparoscopic hysterectomy and myomectomy on clinical outcomes.

NCT ID: NCT03308643 Completed - Myomectomy Clinical Trials

Effect of Oxytocin Infusion on Blood Loss During Abdominal Myomectomy

Start date: October 1, 2017
Phase: Phase 4
Study type: Interventional

To evaluate the effects of oxytocin infusion during abdominal myomectomy.

NCT ID: NCT03250221 Completed - Myomectomy Clinical Trials

Comparison of Robot-assisted Laparoscopic Myomectomy and Traditional Laparoscopic Myomectomy With Barbed Sutures

Start date: March 3, 2017
Phase:
Study type: Observational

To elucidate the impact of barbed sutures on robotic myomectomy and laparoscopic myomectomy

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: NCT02049242 Completed - Uterine Leiomyoma Clinical Trials

Uterine Tourniquet at Open Myomectomy

Start date: January 2014
Phase: N/A
Study type: Interventional

The aim of study is to compare triple tourniquet vs. single tourniquet to reduce blood loss at open myomectomy.

NCT ID: NCT00978601 Completed - Anesthesia Clinical Trials

Improved Recovery Using Multimodal Peri-operative Analgesia in Minimally Invasive Myomectomy

Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate a multimodal analgesic protocol used in minimally invasive surgery for myomectomies (laparoscopic myomectomy (LM) and laparoscopically assisted myomectomy (LAM)).