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Uterine Myoma clinical trials

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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: 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).

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: 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: 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.

NCT ID: NCT01542658 Completed - Uterine Myoma Clinical Trials

Comparison of Robot-assisted Laparoscopic Myomectomy With Traditional Laparoscopic Myomectomy

Start date: February 2012
Phase: N/A
Study type: Observational

This study is to reveal any potential advantage of Robot-assisted Laparoscopic Myomectomy (RLAM) over Traditional Laparoscopic Myomectomy (TLM) by comparing the perioperative variables and short-term outcome of RALM and TLM patients.