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Leiomyoma clinical trials

View clinical trials related to Leiomyoma.

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NCT ID: NCT02192606 Completed - Pelvic Pain Clinical Trials

Does 3D Laparoscopy Improve Vaginal Cuff Suture Time?

3DRCT
Start date: November 2013
Phase: N/A
Study type: Interventional

The objective aim is to evaluate whether the use of 3D laparoscopy facilitates the vaginal cuff closure of the vaginal cuff during a total laparoscopic hysterectomy among novice laparoscopists (PGY 2-4, Fellow). This is a randomized single blinded controlled trial comparing the difference in 2D vs. 3D in regards to vaginal cuff closure time stratified by residents and fellows. Patients will undergo a total laparoscopic hysterectomy and will be randomized to either 2D versus 3D.

NCT ID: NCT02189083 Completed - Leiomyoma Clinical Trials

Study of Tumor-shrinking Decoction (TSD) to Treat Symptomatic Uterine Fibroids

Start date: May 2014
Phase: Phase 3
Study type: Interventional

On the basis of empirical evidence and clinical practice, the investigators have developed a formula called Tumor-shrinking Decoction (TSD) used in the treatment of uterine fibroids (UFs). The investigators preliminary clinical observation has demonstrated the benefits of TSD in improving UFs. TSD is composed of 15 individual Chinese medicines: Astragalus Membranaceus, Semen Coicis, Poria, Curcuma longa L, and Fritillaria Thunbergii Miq, Cassia twig, Pollen typhae, Resina draconis, Lithospermum erythrorhizon, Halloysitum Rubrum, Rhizoma Corydalis processed with vinegar, Hirudo, Calcined corrugated sub , Oyster Shell and Laminaria Japonica Aresch. It is hypothesized that TSD can effectively reduce the fibroid size and improve the symptoms associated with UFs and the greater anti-tumor potency of TSD is associated with higher therapeutic doses. To test this hypothesis, one 16-week, double-blind, randomized, two-dose trial will be conducted in patients with symptomatic UFs to determine whether the high dose (217 g/day) of TSD could produce significantly greater effects in reducing the fibroid size and improving its related symptoms and biochemical profiles compared to the lower dose (69 g/day).

NCT ID: NCT02166411 Completed - Fibroid Clinical Trials

Laparoscopic Myomectomy Using Barbed or Conventional Sutures

Start date: January 2014
Phase: Phase 2
Study type: Interventional

The aim of this study is to compare operative data and early postoperative outcomes of laparoscopic myomectomy using barbed sutures with those of laparoscopic myomectomy using conventional sutures .

NCT ID: NCT02147197 Completed - Leiomyoma Clinical Trials

A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

Start date: March 31, 2014
Phase: Phase 3
Study type: Interventional

This study will evaluate the superiority of ulipristal acetate versus placebo for the treatment of abnormal uterine bleeding associated with uterine fibroids

NCT ID: NCT02147158 Completed - Leiomyoma Clinical Trials

A Study of the Efficacy and Safety of Ulipristal Acetate Intermittent Treatment for Abnormal Uterine Bleeding Associated With Leiomyomas

Start date: January 29, 2014
Phase: Phase 3
Study type: Interventional

This study will evaluate the superiority of ulipristal acetate versus placebo for the treatment of abnormal uterine bleeding associated with uterine fibroids

NCT ID: NCT02131662 Completed - Leiomyoma Clinical Trials

Bay1002670, Fibroids, Safety and Efficacy EU,US,Can, Jap

ASTEROID 1
Start date: May 15, 2014
Phase: Phase 2
Study type: Interventional

The study is performed to assess the efficacy and safety of different doses of BAY1002670 in subjects with uterine fibroids. The dose-response relationship will be evaluated. Further, the study aims to establish a population pharmacokinetic/pharmacodynamic relationship for BAY1002670 in subjects with uterine fibroids. To assess the efficacy of BAY1002670 the interchangeability of menstrual pictogram and alkaline hematin method for the judgement of menstrual blood loss will be assessed.

NCT ID: NCT02123069 Completed - Leiomyoma Clinical Trials

Vascular Function and Uterine Fibroids

Start date: April 2013
Phase: N/A
Study type: Observational

The purpose of this study is to learn how uterine fibroids may be connected to heart disease and high blood pressure. It is not known what causes fibroids, but they frequently occur in women who also have high blood pressure, heart disease, and stroke. The investigators of this study want to learn if certain changes in the blood vessels or nerve activity can put women at risk for these diseases and for fibroids.

NCT ID: NCT02086435 Completed - Uterine Myoma Clinical Trials

Intracorporeal Versus Extracorporeal Morcellation: Clinical Efficacy and Safety Outcomes

IEME
Start date: March 2014
Phase: N/A
Study type: Interventional

The aim of this study protocol will be to compare the technique of intracorporeal morcellation using reusable electronic device (standard technique) with a technique of removal "protected" by endobag and extracorporeal myoma morcellation with cold scissors and scalpel blade or with power morcellator used inside the bag itself.

NCT ID: NCT02086370 Completed - Uterine Fibroids Clinical Trials

Prophylactic Salpingectomy for the Prevention of the Ovarian Cancer: Comparison Between Surgical Techniques

Rad_PBS
Start date: March 2014
Phase: N/A
Study type: Interventional

The aim of this RCT of study is to compare the outcomes of the standard salpingectomy (removal of the fallopian tube) with the radical removal of the tube and the mesosalpinx in terms of ovarian reserve.

NCT ID: NCT02086279 Completed - Endometriosis Clinical Trials

AMH Levels Change During Treatment With GnRh Agonist

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

To evaluate the variation of AMH levels in women undergoing treatment with GnRHa, and to assess whether this variation correlates with changes in the antral and pre-antral follicle ultrasonographic count (AFC).