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Endometriosis clinical trials

View clinical trials related to Endometriosis.

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NCT ID: NCT04669756 Completed - Surgery Clinical Trials

Ovariopexy for Adhesion Prevention After Laparoscopic Removal of Endometriosis of the Pelvic Side Wall or the Ovary

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

prospective randomized Trial comparing ovariopexy over 2, 4 or 6 days vs Placebo after surgery because of endometriosis of the pelvic side wall or the ovary or both

NCT ID: NCT04665414 Completed - Endometriosis Clinical Trials

Diagnosis of Adenomyosis Using Ultrasound, Elastography and MRI

Start date: September 29, 2017
Phase:
Study type: Observational

comparison of transvaginal ultrasound, transvaginal ultrasound elastography and MRI for the diagnosis of adenomyosis in patients receiving hysterectomy afterwards

NCT ID: NCT04664335 Completed - Endometriosis Clinical Trials

Impact of Endometriosis on Pregnancy and Delivery - a Retrospective Cohort Study

Start date: December 1, 2016
Phase:
Study type: Observational

Purpose: To study the impact of endometriosis on subsequent pregnancy and delivery. Methods: retrospective analysis by questionnaire / interview of cases (endometriosis laparoscopically removed / child wish) vs. controls (endometriosis laparoscopically excluded / child wish) from the University Hospital Muenster, Germany, treated between 2009 and 2016; analysis of pregnancy rate, mode of delivery and complications using Clavien-Dindo-classification, role of deep infiltrating endometriosis using ENZIAN classification; data analysis using t-test with p < 0.050% being considered significant.

NCT ID: NCT04650516 Completed - Pain Clinical Trials

Endocare® (Single Care) in Pain-related Endometriosis

Start date: December 3, 2020
Phase: N/A
Study type: Interventional

Endocare® treatment is a stand-alone software medical device, which is composed of a mobile application and an accessory VR headset, intended to mitigate the pain for patients prone to endometriosis.

NCT ID: NCT04639063 Completed - Clinical trials for Endometriosis Outside Pelvis

Assessment of Surgically Removed Abdominal Wall Endometriomas

Start date: October 17, 2020
Phase:
Study type: Observational

A retrospective review of all patients who underwent surgery for an anterior abdominal wall mass which confirmed by pathology examination as an endometrioma will be completely performed. The clinical data will be recorded and pathology report diagnosis will be correlated with the clinical data to assess the possible causes of endometrioma in the women treated in our tertiary hospital and the efficacy of the surgical excision.

NCT ID: NCT04630990 Completed - Endometriosis Clinical Trials

Study Of Oral Elagolix Tablets To Assess the Tolerability and Change in Disease Symptoms in Adult Female Participants With Moderate to Severe Endometriosis-associated Pain

ENDORSE
Start date: December 14, 2020
Phase:
Study type: Observational

Endometriosis is an abnormal, estrogen-dependent growth of endometrial tissue outside the uterus that frequently results in dysmenorrhea and pelvic pain and often causes infertility. Endometriosis is a significant burden on the quality of life of women. This study will assess the tolerability and how effective elagolix is in changing the disease symptoms in adult female participants with endometriosis. Elagolix is an approved drug for treatment of endometriosis. Adult female participants with a diagnosis of endometriosis, who are prescribed elagolix by their physicians, in accordance with local clinical practice and label will be observed for up to 24 months. Around 80 female participants will be enrolled in the study in Israel. Participants will receive Elagolix as prescribed by their physicians. There may be a higher burden for participants in this study compared to standard of care. Patients report outcomes, in the form of questionnaires will be collected up to 24 months prospectively to assess the impact of elagolix on quality of life.

NCT ID: NCT04591548 Completed - Endometriosis Clinical Trials

Biomarkers in Endometriosis

Start date: May 1, 2016
Phase:
Study type: Observational [Patient Registry]

Endometriosis is a common gynecological benign disease which significantly compromise quality of life in patients and is a major cofactor of infertility. With the proteomic approach the investigators will search for proteins with significantly different levels in peritoneal fluid, serum and uterine fluid samples of women with endometriosis versus control group. Results will be validate using ELISA aproach.

NCT ID: NCT04565470 Completed - Endometriosis Clinical Trials

Strategies of Self-management of Endometriosis Symptoms

SAGE
Start date: September 21, 2020
Phase:
Study type: Observational

To determine the prevalence and perceived utility of self-management strategies amongst patients with endometriosis and who consult the endometriosis clinic of the Geneva University Hospital, information about these strategies will be obtained via a web-based questionnaire.

NCT ID: NCT04500743 Completed - Endometriosis Clinical Trials

Role of Suppression of Endometriosis With Progestins Before IVF-ET

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

This study aimed to assess the role of Dienogest pretreatment for endometriosis suppression as compared to Gonadotropin-releasing hormone agonist (GnRHa) in patients with endometriosis pursuing IVF treatment.

NCT ID: NCT04495855 Completed - Endometriosis Clinical Trials

A Study to Learn More About Using Dienogest to Treat Endometriosis in Chinese Participants

VISANNE OS
Start date: October 28, 2020
Phase:
Study type: Observational

Endometriosis is a condition that affects women, usually during their reproductive years. In women with endometriosis, the tissue that lines the uterus starts to grow outside of the uterus. This can cause pain during their periods or during sex, and constant pain in the pelvis. Endometriosis can decrease a woman's quality of life and requires long-term treatment to control the symptoms. For some women with endometriosis, symptoms can return after they stop treatment. Or, they may not be able to tolerate the current long-term treatment options. In this study, researchers will find out more about the safety of long-term treatment with dienogest in a large number of Chinese participants. This study will enroll patients from post-menarche to menopause with clinically or surgically diagnosed endometriosis. All of the participants will take dienogest based on their doctor's instructions. They will then visit their doctor's office 3 times over 6 months. During these visits, their doctors will ask them if they have any health problems and about their quality of life. Their doctors will also do tests to measure the pain caused by their endometriosis and any other symptoms.