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Leiomyoma clinical trials

View clinical trials related to Leiomyoma.

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NCT ID: NCT05025410 Completed - Myoma;Uterus Clinical Trials

Remimazolam and Remifentanil Without Neuromuscular Blocking Agent

Start date: November 1, 2021
Phase:
Study type: Observational

Remimazolam is a novel drug approved for induction and maintenance of general anesthesia. This study aims to check the appropriate dose and patient response by administering remimazolam and remifentanil in surgery that does not require a neuromuscular blocking agents.

NCT ID: NCT04996498 Completed - Leiomyoma Clinical Trials

Hemostatic Effect of Intrauterine Instillation of Oxytocin in Hysteroscopic Myomectomy

oxytocin
Start date: April 15, 2021
Phase: N/A
Study type: Interventional

There is no previous study on the hemostatic effect of intrauterine instillation of oxytocin in hysteroscopic myomectomy. All previous studies focused on intravenous administration of oxytocin. This trial may modify the surgical environment in hysteroscopic myomectomy by decreasing intraoperative bleeding to a degree that the amount of distention medium required for uterine distention will be reduced with a better visibility and shorter operation time. The standard treatment of symptomatic myomas is hysterectomy for women who have completed childbearing period, and myomectomy for women who wish to preserve fertility hysteroscopic myomectomy currently is the gold standard minimally invasive procedure for the management of symptomatic submucous fibroids. Success of hysteroscopic myomectomy depends on good visualization throughout the procedure, via the correct distending pressure, continuous irrigation and the use of electrosurgery to control bleeding. Prolonged procedures that need continuous irrigation under high pressure are associated with higher risk of excessive fluid absorption and intravasation syndrome due to opened blood vessels within the myometrial, moreover, the thermal damage of the healthy tissues is increased with the use of the coagulation current. Oxytocin receptors exist in the non-pregnant uterus but the concentration of the receptors is much lower than in pregnancy. this is why the clinical use of oxytocin outside of pregnancy is limited Oxytocin acts on oxytocin receptors in the myometrium and fibroid tissue leading to uterine contraction and constriction of uterine vasculature due to uterine contraction and vaso-constrictive effect of oxytocin thus reducing uterine perfusion and results in reducing intraoperative bleeding.

NCT ID: NCT04874246 Completed - Uterine Leiomyoma Clinical Trials

Comparison of Concentration of Vasopressin During Robot-assisted Laparoscopic Myomectomy

VALENTINE
Start date: May 10, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of the concentration of vasopressin, which is used as a method for reducing blood loss in robot-assisted laparoscopic myomectomy.

NCT ID: NCT04832906 Completed - Uterine Fibroid Clinical Trials

UA Versus UAE in Treatment of Fibroids

Start date: March 13, 2019
Phase: Phase 4
Study type: Interventional

Study objective: To prove that Ulipristal acetate is an effective line of management for uterine fibroids by causing a significant decline in fibroid volumes resulting in a substantial relief of fibroid-related symptoms, and to compare its results with those of uterine artery embolization. Design: A randomized control trial. Setting: Maternity Hospital, Ain Shams University. Patients: Women with symptomatic uterine fibroids. Interventions: 70 women were randomly assigned to either Ulipristal Acetate (UA) group or uterine artery embolization (UAE) group (35 in each group). Both groups were followed up to detect the decline in fibroid size as well as the improvement of symptoms.

NCT ID: NCT04819633 Completed - Uterine Leiomyoma Clinical Trials

Evaluating Serum Sestrin in Leiomyoma Patients

Start date: January 1, 2021
Phase:
Study type: Observational

Leiomyomas are the most common benign neoplasms of women's reproductive system affecting 20-30% of women within the reproductive ages. Sestrins are serum proteins which are highly expressed under circumstances of DNA damage, hypoxia and oxditive stress and play an important role in autophagia. The aim of this study is to evaluate the relationship of serum sestrin proteins with development of leiomyomas.

NCT ID: NCT04762316 Completed - Clinical trials for Uterine Fibroids Affecting Pregnancy

Composition for Treating Uterine Fibroid (PP6)

PP6
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Pregnenolone & Pyridoxal Phosphate (PP6) for treating uterine fibroids in women pregnancy to lost the size fibroids and to dissolve fibroids. Uterine fibroids are a very common finding in women pregnancy of reproductive age, fibroids fast grow in the first trimester pregnancy. PP6 against the rapid growth of fibroids under the influence of hormones during pregnancy. Use to PP6 think about regulating stable Oestrogen level and to dissolve fibroids. This is a substantial insight into the pathogenesis of disease, with a clear path toward clinical application, or which would lead to a substantial advance and perfect in management or public health policy.

NCT ID: NCT04736095 Completed - Fibroid Clinical Trials

3 Dimensional Ultrasound in Comparison to Hysteroscopy in Myomas

Start date: February 7, 2021
Phase:
Study type: Observational

• three-dimensional saline infusion sonohysterography (3D SIS) was performed in all cases. A sterile Cuscoe speculum was passed, the cervix visualized and cleaned with sterile chlorhexidine solution. A 3.3 mm soft plastic paediatric naso-gastric suction catheter was then passed through the cervix into the uterine cavity without grasping the cervix.

NCT ID: NCT04672421 Completed - Laparoscopy Clinical Trials

The Efficacy and Safety of Medicurtain® in Patients With Total Laparoscopic Hysterectomy (Pivotal Study)

Start date: April 18, 2011
Phase: N/A
Study type: Interventional

This study was designed to assess the safety and efficacy of MEDICURTAIN. Patients who underwent total laparoscopic hysterectomy were randomly assigned either into Medicurtain® treatment group or non-treatment control group. Adhesion formations at 8 weeks after the index surgery were compared between the two groups by using the well-defined grade scale and image recording.

NCT ID: NCT04576039 Completed - Uterine Fibroid Clinical Trials

Ultrasonographic Appearance of the Endometrium After Ulipristalacetate Use and Endometrial Changes

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

If endometrial thickening is visualised (>10mm) after the use of ulipristalacetate in case of medical treatment for uterine fibroids a saline infusion and sonographic examination will be performed to evaluate the endometrium and exclude intra-uterine pathology.

NCT ID: NCT04550429 Completed - Fibroids Clinical Trials

Uterine Filling Pressure in Hysteroscopy

Start date: August 21, 2020
Phase: N/A
Study type: Interventional

The aim of the study is to compare the outcomes of patients undergoing hysteroscopy with a Myosure device with a pressure of 60 mmHg to those using the standard of 80 mmHg.