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Bowel Endometriosis clinical trials

View clinical trials related to Bowel Endometriosis.

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NCT ID: NCT05291624 Recruiting - Endometriosis Clinical Trials

Ultrasonographic and Surgical Assessment of Endometriosis by AAGL 2021 Endometriosis Classification

ULTRA-AAGL
Start date: April 1, 2022
Phase:
Study type: Observational

In 2021, an international consensus developed a new endometriosis classification system, called AAGL 2021 Endometriosis Classification, for scoring intraoperative surgical complexity and to examine its correlation with patient-reported pain and infertility. Until now, no study has investigated the role of AAGL 2021 Endometriosis Classification in ultrasonographic assessment of patient with endometriosis. This study aims to compare the use of the AAGL 2021 Endometriosis Classification in preoperative (at ultrasound) and intraoperative (at surgery) evaluation of patients with endometriosis.

NCT ID: NCT04669769 Completed - Endometriosis Clinical Trials

Retrospective Analysis of Results of Surgery for Deep Bowel Endometriosis

Start date: December 1, 2019
Phase:
Study type: Observational

identification of patients operated becaus of bowel endometriosis at the endometriosis center, University Hospital Muenster, Germany, starting 2009, Analysis of Patient history, surgical procedurie, intraoperative complications, postoperative complications, phone call assessing further complications, complaints after surgery, pregnancy, live birth, additional surgery, spontaneous conception, conception by IUI, ART

NCT ID: NCT04338035 Completed - Endometriosis Clinical Trials

Fertility in Untreated Rectosigmoid Endometriosis

Start date: May 1, 2009
Phase:
Study type: Observational

Several studies investigated the reproductive outcomes after surgical treatment of colorectal endometriosis, mainly segmental colorectal resection. Little information is available on the spontaneous fertility of patients with bowel endometriosis. This study aims to evaluate the fertility of patients affected by rectosigmoid endometriosis who did not undergo previous surgical treatment.

NCT ID: NCT03565848 Not yet recruiting - Endometriosis Clinical Trials

Mesenteric Sparing Surgery in Laparoscopic Colorectal Resection for Endometriosis

IRE-1
Start date: May 1, 2022
Phase:
Study type: Observational

Colorectal resection is a standard surgical treatment of bowel deep infiltrating endometriosis (DIE). Nevertheless, concerns about different bowel functional outcomes related to radical surgery versus conservative surgery as shaving technique is a topic leading to much debate. Different surgical approach are used to perform colorectal resection and there is not a standardized technique. For the same concerns, studies have addressed the mesenteric vascular and nerve preservation both in oncological and benign intestinal disease with improved functional outcome. Therefore, the aim of this prospective study is to analyze feasibility and safety of mesenteric vascular and nerve Sparing Surgery in laparoscopic segmental colorectal resection for DIE with short and long term follow up. Women with DIE ,that underwent laparoscopic segmental colorectal resection, will undergo resection performed with inferior mesenteric artery and branching arteries preservation by dissecting adherent to the intestinal wall with mesenteric vascularization and innervation entirely preserved. Personal history, clinical data, surgical data, short and long term surgical complications and long term outcomes will be recorded. Symptoms and bowel function will be evaluated before and after surgery.

NCT ID: NCT03532074 Recruiting - Clinical trials for Endometriosis, Rectum

Indocyanine Green and Rectosigmoid Endometriosis

vincendo
Start date: May 28, 2018
Phase: N/A
Study type: Interventional

Indocyanine green is a fluorescent dye used for the intraoperative evaluation of tissue perfusion. The aim of this study is to evaluate a possible correlation between rectosigmoid vascularization and surgical and clinical data including pre and post-operative bowel symptoms in patients needing surgery for rectosigmoid endometriosis.

NCT ID: NCT02547909 Withdrawn - Bowel Endometriosis Clinical Trials

The Application of Probe-based Confocal Laser Endomicroscopy in the Diagnosis of Deep Endometriosis

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

Endometriosis is defined as the presence of endometrial glands and stroma outside of the uterus.Endometriosis affects 5%-15% of women in the reproductive age. Deep endometriosis is mostly defined as a single endometrial nodule, located in the vesico-uterine fold or close to the distal 20 cm of the large bowel. Current guidelines recommends that laparoscopy with histology should be done to diagnose endometriosis. Probe-based confocal laser endomicroscopy (pCLE) has been used as a GI tract endoscopy additive tool in recent years, providing in-vivo cellular-level imaging, a concept known as "optical biopsy". considering the rectal bleeding that occurs in patients suffering from bowel endometriosis, usually with a normal mucosa seen at standard endoscopy (personal data), we hypothesized that there might be histological architectural changes in the vessels or the mucosa/sub mucosa in bowel endometriosis.

NCT ID: NCT02102529 Completed - Bowel Endometriosis Clinical Trials

Survey: Clinical Outcome After Bowel Resection in Women Due to Endometriosis

Start date: April 2014
Phase:
Study type: Observational

Endometriosis is one of the most frequent benign diseases that can affect women in their reproductive age. In severe form, the colon or rectum may be involved. It has been shown that the surgical treatment improve typical symptoms like pain and dyspareunia. The investigators evaluated the functional results and quality of life after laparoscopic colonic resection for endometriosis

NCT ID: NCT02100345 Completed - Bowel Endometriosis Clinical Trials

Conservative Treatment of Rectosigmoid Endometriosis Monitored by Transvaginal Ultrasound

Start date: October 2014
Phase: N/A
Study type: Observational

Background: Endometriosis is a disease affecting 8-15 % of fertile women and is a cause of abdominal pain and suffering during women's menstrual periods. A subgroup of patients with DIE has an infiltration into the rectosigmoid bowel wall (4-37%). Knowledge of the growth pattern of rectosigmoid lesions related to subjective symptoms is mandatory in order to assess the need for follow-up with transvaginal ultrasound during medical treatment. Hypotheses: Symptoms will follow growth of rectosigmoid endometriosis. Material and methods: Two different cohorts of women, based on time of diagnosis of rectosigmoid endometriosis and treatment with hormonal intrauterine device or continuous oral contraceptives will receive a questionnaire and a transvaginal ultrasound scan (measuring size and volume) at inclusion, (6) and 12 months later. Perspectives: Patients treated conservatively may be followed by questionnaires, thereby reducing the need for time consuming clinical controls.