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Leiomyoma clinical trials

View clinical trials related to Leiomyoma.

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NCT ID: NCT02061657 Completed - Leiomyoma Clinical Trials

Impact of Misoprostol on Blood Loss In Myomectomy Operations

Start date: June 2013
Phase: Phase 3
Study type: Interventional

The aim of this research work is to assess the effect of using single preoperative dose of rectal misoprostol in abdominal myomectomy operations on blood loss, duration of the operation and possible operative complications

NCT ID: NCT02059954 Completed - Uterine Fibroids Clinical Trials

Vaginal vs. Laparoscopic Hysterectomy

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

Hysterectomy for benign indication is one of the most common surgical procedures in women. Numerous reviews and guidelines recommend the vaginal approach for benign hysterectomy, but the proportion of laparoscopic (and robotic) hysterectomies is increasing. This study will compare a range of clinical and subjective outcomes of vaginal vs. total laparoscopic hysterectomy. Outcomes include operating time, postoperative recovery, return to work as well as cosmesis, quality of life and sexual health.

NCT ID: NCT02056717 Completed - Adenomyosis Clinical Trials

Use of Dexamethasone in Uterine Artery Embolization

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

The primary purpose of this study is to investigate the effects of dexamethasone on inflammatory reactions after uterine artery embolization. The secondary purpose of this study it to investigate the effects of dexamethasone on postembolization syndrome (severe pain, nasea and vomiting).

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: NCT01992718 Completed - Uterine Fibroids Clinical Trials

What Are we Missing? Diagnosing Uterine Adenomyosis Using Ultrasound Elastography

Start date: November 2013
Phase: Early Phase 1
Study type: Interventional

To improve the clinical care of women with pelvic pain and abnormal uterine bleeding due to benign uterine conditions including leiomyomas (uterine fibroids) and adenomyosis by evaluating the accuracy of radiology diagnostic exams (MRI(magnetic resonance imaging), ultrasound and ultrasound with elastography).

NCT ID: NCT01984632 Completed - Uterine Myoma Clinical Trials

Barbed Suture in Single-port Laparoscopic Myomectomy

Start date: November 2013
Phase: Phase 3
Study type: Interventional

The aim of this study is to test our hypothesis that the use of unidirectional knotless barbed suture in single-port laparoscopic myomectomy could facilitate the suture of uterine wall defect after myoma enucleation as multi-port laparoscopic myomectomy did.

NCT ID: NCT01946178 Completed - Clinical trials for Uterine Fibroids (Leiomyomas)

Clinical Study of the Mirabilis High-Intensity Focused Ultrasound System for Non-Invasive Treatment of Uterine Fibroids

Start date: January 2011
Phase: N/A
Study type: Interventional

The Mirabilis High-Intensity Focused Ultrasound (HIFU) Treatment System delivers therapeutic focused ultrasound energy to the uterus under integrated ultrasound imaging guidance to offer non-invasive treatment for uterine fibroids. The purpose of this clinical study is to assess the initial safety and performance of the Mirabilis HIFU Treatment System for transabdominal treatment of uterine fibroids in eligible women who are scheduled to undergo hysterectomy following treatment with the device or who are seeking relief from fibroid-related symptoms.

NCT ID: NCT01937104 Completed - Ovarian Cancer Clinical Trials

ONSD According to the Position During Laparoscopy

ONSD
Start date: September 2013
Phase: N/A
Study type: Interventional

Increase of intracerebral pressure (ICP) during laparoscopic surgery has known to be associated with positional changes. Optic nerve sheath diameter (ONSD) has correlation with ICP and ultrasonographic measurement of optic nerve sheath diameter (ONSD) is known to be a noninvasive and rapidly applicable technique for evaluating ICP. The aim of this study is to investigate the change of ONSD according to the positional change during laparoscopic surgery.

NCT ID: NCT01936493 Completed - Uterine Fibroids Clinical Trials

Biologic Predictors of Leiomyoma Treatment Outcomes

Start date: August 2009
Phase: N/A
Study type: Observational

The purpose of this study is to search for the hereditary (genetic) causes of uterine fibroids. Some women with uterine fibroids may have one or more genes that make them more likely to develop uterine fibroids. We are trying to identify these genes to better understand how and why uterine fibroids develop and to design better treatment options for women with uterine fibroids. This information may also help us to understand and treat other problems that may be caused by these genes.

NCT ID: NCT01873378 Completed - Uterine Myoma Clinical Trials

GnRH Agonist Pretreatment in Hysteroscopic Myomectomy

Start date: January 2013
Phase: N/A
Study type: Interventional

The primary outcome of this study is to assess if the GnRHa administration before cold loop hysteroscopic myomectomy contributes to accomplish the treatment in only one surgical procedure. Moreover, we will investigate the intraoperative influence of such pharmacologic therapy in terms of distension liquid absorption and duration of the procedures.