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Pelvic Surgery clinical trials

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NCT ID: NCT04561414 Withdrawn - Clinical trials for Lower Abdominal Surgery

Objective to Evaluate the Safety and Effectiveness of LED Light Source System for Endoscopy in Ureteral Radiography

IRIS
Start date: May 2021
Phase: N/A
Study type: Interventional

This clinical trial is a prospective, multi-center, single-blind, parallel, randomized controlled superiority clinical trial. The trial will be carried out in 5 centers, involving 120 subjects as estimated who will be divided into the test group or control group randomly on an equal basis (each group includes 60 subjects). This trial will be carried out in 4 stages, including the screening period, random grouping, operation date and follow-up period. In the screening period, the informed consent forms are collected and candidates are screened; after screening, the accepted subjects will be randomly divided into the control group or test group; on the operation date, the operation is carried out using the device tested; safety follow-up visit is carried out during the follow-up period.

NCT ID: NCT03535428 Completed - Clinical trials for Venous Thromboembolism

Venous Thrombo-embolic Complication prévention in Pelvic Surgery

Start date: February 13, 2017
Phase:
Study type: Observational

Pelvic fracture surgery are very high thrombotic risk surgery with about 10% to 50% venous thrombo embolic complications and 0.5% to 10% of pulmonary embolism. The ST JOSEPH's Hospital have almost 60 cases per year . Following a fatal pulmonary embolism per operatory the team has set up a venous exploratory protocol before surgery. This protocol includes a venous doppler ultrasound of lower limbs associated to a abdo pelvic scanner in the 48hours before surgery. The aim is to evaluate this new protocol efficacy on prevention of thrombo embolic complications in pelvic fracture surgery.

NCT ID: NCT03469570 Completed - Abdominal Surgery Clinical Trials

Assisted Fluid Management IDE Study

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

The primary objective of this study is to evaluate the performance of the Acumen™ Assisted Fluid Management (AFM) Feature in its ability to predict a subject's fluid responsiveness.

NCT ID: NCT02669498 Completed - Pelvic Surgery Clinical Trials

Consequences of Changing Current Standards: Endocrine Status After Routine Fallopian Tube Removal

Start date: November 2013
Phase: N/A
Study type: Interventional

Two recently published articles need to be cited to explain the rationale for our study since both studies conclude with contrary findings: The first one is "The post-reproductive Fallopian tube: better removed?" and the other is termed "Factors associated with age of onset and type of menopause in a cohort of UK women". In essence, while Dietl et al suggest to remove the Fallopian tube routinely in every hysterectomy and every sterilization procedure after 35 yrs of age, Pokoradi et al showed that pelvic surgical procedures and even simple tubal sterilization are associated with an earlier menopause. Hence, this is an important issue as early menopause leads to adverse health status.