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Leiomyoma clinical trials

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NCT ID: NCT03533907 Completed - Infertility, Female Clinical Trials

Pregnancy Outcomes in Infertile Patients After Treatment With Ulipristal Acetate.

Start date: November 1, 2013
Phase:
Study type: Observational

The investigators analyzed a group of infertile women treated with Ulipristal Acetate (UA) for uterine fibroids at the Humanitas Fertility Center. All the patients' data were extracted from the Fertility Center external-audit-anonymized electronic research query system.

NCT ID: NCT03444987 Completed - Uterine Fibroid Clinical Trials

The Role of Fibroblast Activation in Uterine Fibroid

Start date: March 1, 2018
Phase:
Study type: Observational

Uterine fibroids (UFs), also called uterine leiomyomas or myomas, are steroid hormone-responsive, benign tumors of the smooth muscle compartment (myometrium) of the uterus. They are the most common neoplasm affecting women in their reproductive age. It is estimated that up to 77% of women develop UF in their life. UFs are one of the leading causes of hospitalisations for gynaecological disorders and are the most frequent reason for hysterectomy. According to relevant literature, 40%-60% of all the hysterectomies performed are due to the presence of UFs.

NCT ID: NCT03427671 Completed - Leiomyoma Clinical Trials

OCL 500 Treatment of Women With Symptomatic Uterine Fibroids

Start date: January 17, 2018
Phase: N/A
Study type: Interventional

This is a prospective, open-label, single-arm, safety and effectiveness study of Occlusin 500 microspheres in women with symptomatic uterine fibroids.

NCT ID: NCT03420248 Completed - Leiomyoma Clinical Trials

Comparison of Pain of Two Different Methods in Uterine Artery Embolization

Start date: April 19, 2018
Phase: N/A
Study type: Interventional

The primary purpose of this study is to compare pain after uterine artery embolization using non-spherical polyvinyl alcohol particles or tris-acryl gelatin microsphere in patients with symptomatic fibroids

NCT ID: NCT03412890 Completed - Uterine Fibroid Clinical Trials

LIBERTY EXTENSION: Efficacy and Safety Extension Study of Relugolix in Women With Heavy Menstrual Bleeding Associated With Uterine Fibroids

Start date: October 19, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study was to determine the long-term efficacy and safety of relugolix 40 milligrams (mg) once daily co-administered with estradiol (E2) and norethindrone acetate (NETA) for 28 weeks on heavy menstrual bleeding associated with uterine fibroids in participants who previously completed a 24-week treatment period in one of the pivotal studies (MVT-601-3001 or MVT-601-3002).

NCT ID: NCT03411980 Completed - Endometriosis Clinical Trials

Pharmacokinetics and Safety of Vilaprisan in Renal Impairment

Start date: February 2, 2018
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the pharmacokinetics of vilaprisan in subjects with moderate to severe renal impairment compared with matched subjects with normal renal function.

NCT ID: NCT03349190 Completed - Infertility, Female Clinical Trials

Impact of Esmya on Fertility to Infertile Women With Fibroids Managed With Assisted Reproduction Techniques

NACRE
Start date: December 29, 2017
Phase:
Study type: Observational

Fibroid is a frequent pathology of infertile women. Its deleterious effect on the infertility would be due to the mechanical way. The interest of the resection of intramural fibroids is discussed. It is necessary to measure the indication of a myomectomy, whatever the surgical procedure. On the one hand, it may cause important potential complications, and on the other hand, the surgery does not improve the parameters of the fertility. Thus, it is a major stake to avoid the surgical operation. A decrease of the size of these fibroids by medical treatment is then a good option. When the surgical treatment is necessary, a medical pre-surgical treatment is often proposed in order to decrease the symptomatology and to reduce the size of the fibroid to facilitate the surgery. Acetate Ulipristal (UPA) has been marketed in this indication. Following the Pearl I-II studies, the first indication in France was a pre-surgical treatment for 3 months at a dose of 5 mg per day. The Pearl III and IV studies evaluated the Esmya® administration as a long-term intermittent repeated treatment, giving to it a prominent position for the long-term management of symptomatic fibroids. Furthermore, cases of pregnancy before surgery are frequently described in women with fibroids treated by UPA for a pre-IVF surgery. 5 to 10 % of women who are managed for infertility have fibroids and only 2% to 3% have this unique cause of infertility. Then, some of patients followed in ART centers have been treated by UPA to reduce the fibroids size and/or to decrease the associate symptoms. The aim of this study is to evaluate in the different French ART centers, the impact on fertilization of UPA administration for infertile women with fibroids and to describe the modalities of its prescriptions and to collect information regarding safety tolerance profile of Esmya® in this patient population.

NCT ID: NCT03328260 Completed - Uterine Leiomyoma Clinical Trials

High Intensity Focused Ultrasound in Uterine Myoma

Start date: December 12, 2017
Phase: N/A
Study type: Interventional

Aim to evaluate the efficacy of safety of newly developed, high intensity focused ultrasound device in women with symptomatic uterine leiomyoma

NCT ID: NCT03317795 Completed - Uterine Fibroids Clinical Trials

Treatment of Heavy Menstrual Bleeding in Women With Uterine Fibroids

Start date: November 14, 2017
Phase: Phase 4
Study type: Interventional

This is a randomized controlled trial (RCT) to assess the comparative effectiveness of Levonorgestrel Intrauterine System (LNG-IUS) to Tranexamic Acid (TA) for the treatment of heavy menstrual bleeding (HMB) in women with clinically-significant fibroids.

NCT ID: NCT03270605 Completed - Cesarean Section Clinical Trials

Myomectomy During CS: A Retrospective Cohort Study

Start date: January 1, 2015
Phase:
Study type: Observational

To evaluate the value of myomectomy during delivery by cesarean section (CS) in pregnant women with uterine fibroids.