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Endometriosis clinical trials

View clinical trials related to Endometriosis.

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NCT ID: NCT03080558 Recruiting - Deep Endometriosis Clinical Trials

Estimation of Vascularization After Treatment of Deep Rectovaginal Endometriosis Node by Rectal Shaving

INDIE
Start date: August 6, 2017
Phase: Phase 4
Study type: Interventional

Indocyanine green is a dye, using in surgery to bring out the intraoperative evaluation of tissue perfusion. After intravenous injection of indocyanine green, using a near infrared light, the vascularisation becomes fluorescent. In endometriosis disease, the treatment of recto vaginal node can be complicated by rectovaginal fistula. An abnormal vascularisation related to the surgery would be a risk factor of post operative fistulas. The aim of this study is to evaluate the rectal and vaginal vascularisation during the treatment of a recto vaginal endometriosis nodule with rectal shaving, using indocyanine green fluorescence.

NCT ID: NCT03006406 Recruiting - Clinical trials for Clinical Pregnancy Rate

Effect of Shorten Gonadotropin-releasing Hormone Agonist Therapy on the Outcome of in Vitro Fertilization-Embryo Transfer in Patients With Endometriosis

Start date: January 2016
Phase: N/A
Study type: Interventional

Gonadotropin-releasing hormone analogue (GnRH-a) is a synthetic decapeptide compound which can down-regulate pituitary function causing a temporary low estrogen state. Since endometriosis is an estrogen-dependent disease, the use of long-acting GnRH-a can control the growth of endometriosis by inhibiting ovary function.Some scholars have found that, for adenomyosis patients who received a super long protocol (pretreatment of long-acting GnRH-a for 1-2 months) in IVF treatment, the pregnancy outcome is comparable to that of the controls with normal uterus. Thus, the aim of this study is to compare the clinical pregnancy rate in patients treated with GnRH-a for 1, or 2 months.

NCT ID: NCT02975219 Recruiting - Endometriosis Clinical Trials

Feasibility Study of Using Molecular Fluorescence Guided Surgery in Endometriosis

Endo-light
Start date: May 1, 2017
Phase: Phase 1
Study type: Interventional

Incomplete resection of endometriosis lesions often results in recurrence of symptoms and the need for repeated surgery, with considerable associated morbidity. The aim of this pilot project is to determine the feasibility of fluorescence imaging to improve the treatment of endometriosis in the future.

NCT ID: NCT02958423 Recruiting - Endometriosis Clinical Trials

tDCS Versus tsDCS for Endometriosis-related Chronic Pelvic Pain Treatment

DCSErCPP
Start date: November 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to compare the analgesic effect of 2 mA anodal direct current stimulation on the right primary motor cortex (M1) (tDCS) with a similar stimulation on the spine (D10) (tsDCS) in healthy volunteers (HV) followed by a pilot study in patients suffering of endometriosis-related chronic pelvic pain (CPP)

NCT ID: NCT02948972 Recruiting - Infertility Clinical Trials

Impact of Complete Surgery of Colorectal Deep Infiltrating Endometriosis on Fertility

ENDOFERT
Start date: November 17, 2016
Phase: N/A
Study type: Interventional

The ENDOFERT Study is an open, multicenter, randomized, parallel-group, controlled trial. This study includes patients presenting colorectal DIE and infertility. Patients will be randomized in two parallel-groups; one group underwent complete surgery of colorectal DIE prior to ART and the other group underwent ART alone (ratio 1:1)

NCT ID: NCT02793908 Recruiting - Endometriosis Clinical Trials

Subcutaneous Progesterone Supplementation in Patients With Endometriosis

PleyrisEndom
Start date: June 2016
Phase: Phase 3
Study type: Interventional

The aim of the study protocol will be to compare the efficacy of subcutaneous progesterone (25 mg / day; Pleyris, IBSA Institut Biochimique SA) with vaginal progesterone (90 mg / day; Crinone, Merck Serono) administered during the luteal phase in term of pelvic pain reduction in patients with grade I-II endometriosis and / or endometrioma <4 cm subjected to time intercourses or COS/IUI cycles.

NCT ID: NCT02676713 Recruiting - Infertility Clinical Trials

Traditional Chinese Medicine Sequential Treatment for Endometriosis Associated Infertility

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

Endometriosis is a common, chronic disease. 30% to 50% of women with endometriosis are infertile. There is moderate quality evidence that laparoscopic surgery to treat mild and moderate endometriosis increases live birth or ongoing pregnancy rates. There was no evidence of benefit for post-surgical hormonal suppression of endometriosis compared to surgery alone for the outcomes of pregnancy rates. Past studies have confirmed that Chinese herbal medicine can inhibit post-surgical endometriosis recurrence, increase pregnancy rate.This study evaluates the efficacy and safety of Traditional Chinese Medicine Sequential Treatment of endometriosis-associated infertility. The study objective is to confirm that clinical pregnancy rate of patients with endometriosis-associated infertility post-conservative surgery accepting Chinese medicine activating blood, dredging liver and nourishing kidney sequential treatment is higher than expectant treatment.

NCT ID: NCT02623244 Recruiting - Clinical trials for Ovarian Endometrioma

The Association Between Ovarian Endometrioma and Lower Urinary Tract Symptoms

Start date: November 15, 2015
Phase:
Study type: Observational

To assess the relationship between ovarian endometrioma and lower urinary tract symptoms, sexual function and gastrointestinal symptoms. In addition, the investigators also assess the impact of surgeries for ovarian endometrioma on lower urinary tract symptoms, sexual function and gastrointestinal symptoms.

NCT ID: NCT02575248 Recruiting - Infertility Clinical Trials

Induction of Ovulation by Clomiphene Citrate Following Laparoscopic Surgery for Endometriosis Stage 1 and Stage 2 With and Without Suppression by Dienogest

Start date: October 2014
Phase: Phase 4
Study type: Interventional

This study aims at investigating the fertility outcome of endometriosis suppression with dienogest 2mg / day for 3 month followed by induction of ovulation for 3 month in endometriosis patients stage I and II.

NCT ID: NCT02481739 Recruiting - Endometriosis Clinical Trials

Laparoscopic Surgical Management of Endometriosis on Fertility

Start date: September 2015
Phase: N/A
Study type: Observational

The aim of the investigators study is to know the results of the endometriosis surgery and particularly to highlight a benefit of this surgery on fertility.