Clinical Trials Logo

Uterine Myoma clinical trials

View clinical trials related to Uterine Myoma.

Filter by:

NCT ID: NCT06099977 Recruiting - Prostate Cancer Clinical Trials

Binaural Sound for Remimazolam Induction

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

It is important to decrease the time-to-loss of consciousness and anesthetics dose of remimazolam for general anesthesia induction. We will evaluate the effect of binaural sound for general anestheia induction using remimazolam infusion.

NCT ID: NCT05108597 Completed - Clinical trials for Blood Loss, Surgical

Effect of Rectal Misoprostol in Reducing Intra-operative Blood Loss During Myomectomy

Start date: March 4, 2019
Phase: Phase 3
Study type: Interventional

A total of 200 women for elective abdominal myomectomy were randomly allocated into two groups. 100 women in experimental group were administered 400ug Misoprostol (2 tablets of Prosotec®) through the rectal route prior to surgery and 100 were in control group, in which no drug was administered.

NCT ID: NCT05086770 Completed - Uterine Fibroid Clinical Trials

Comparison of Pain After Uterine Artery Embolization Using Gelatin Microsphere or Tris-acryl Gelatin Microsphere

Start date: May 31, 2021
Phase: N/A
Study type: Interventional

This study is a prospective and randomized investigation planned to compare pain after uterine artery embolization using Gelatin microsphere or tris-acryl gelatin microsphere in 60 patients with symptomatic fibroids.

NCT ID: NCT04279626 Completed - Uterine Myoma Clinical Trials

Surgical Outcome of Two-port Laparoscopic Myomectomy

Start date: January 21, 2015
Phase:
Study type: Observational

Study Objective: To evaluate the surgical outcome of laparoendoscopic two-sites myomectomy (LETS-M) and compare the difference between an experienced surgeon and three trainees. Design: A retrospective study. Setting: A university hospital and a tertiary care center. Patients: 204 women underwent LETS-M

NCT ID: NCT03156127 Withdrawn - Uterine Myoma Clinical Trials

A Study to Compare the Pharmacokinetics and Safety/Tolerability of BR-UPS (Ulipristal Acetate) 5 mg Tablet With Inisia (Ulipristal Acetate) 5 mg Tablet

Start date: May 19, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the Pharmacokinetics and Safety / Tolerability of BR-UPS (Ulipristal acetate) 5 mg tablet with Inisia (Ulipristal acetate) 5 mg tablet in healthy female volunteers

NCT ID: NCT02631278 Recruiting - Uterine Myoma Clinical Trials

Radio Frequency Ablation (RFA STUDY )

RFA
Start date: December 2014
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the safety and feasibility of a radiofrequency (RF) system employing RFITT (CelonProSurge) probes for the ablative treatment of uterine fibroids.

NCT ID: NCT02563392 Recruiting - Uterine Myoma Clinical Trials

Does Preventive Uterine Artery Occlusion During Laparoscopic Myomectomy Impact on Ovarian Reserve Markers?

ORAM
Start date: April 2015
Phase: N/A
Study type: Interventional

Hysterectomy is an effective treatment used as a first-line approach for uterine myomas. Several others alternatives to hysterectomy have been developed in recent years for women wishing to retain their uterus: myomectomy, radiological embolization, focused ultrasound. Myomectomy, particularly through minimally invasive surgery, is currently considered the conservative treatment of choice for patients wishing to preserve their fertility. However, three important issues should be considered: the risk of intra- and postoperative bleeding, the risk for recurring myomas, and the preservation of subsequent fertility. Preventive uterine artery occlusion can be combined with laparoscopic myomectomy in order to avoid bleeding and improve uterine suture. Another expected long-term benefit is the improvement of treatment efficacy, leading to less symptoms and myomas recurrence. However, the effect of uterine arteries occlusion on the ovarian reserve of women of childbearing age has not yet been studied, which limits its clinical application.

NCT ID: NCT02392585 Completed - Uterine Myoma Clinical Trials

Single or Triple Uterine Tourniquet at Myomectomy

Start date: March 2015
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: 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: 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).