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Bariatric Surgery clinical trials

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NCT ID: NCT03184285 Completed - Bariatric Surgery Clinical Trials

Continuous Non-invasive Assessment of Blood Pressure in Bariatric Surgery

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

Comparability of discontinuous non-invasive (sphygomanometric) and continuous semi-invasive and invasive (Masimo© ; Nexfin© Monitoring ; FloTrac© Edwards Lifesciences) beat to beat measurement methods for the determination of arterial blood pressure in patients undergoing bariatric surgery.

NCT ID: NCT03184272 Completed - Bariatric Surgery Clinical Trials

Non-invasive Assessment of Cardiac Output and Fluid Responsiveness in Bariatric Surgery

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

Comparability of discontinuous non-invasive (sphygomanometric) and continuous semi-invasive and invasive (Masimo©; Nexfin© Monitoring ; FloTrac © Edwards Lifesciences) beat to beat measurement methods for the determination of cardiac output and fluid responsiveness in patients undergoing bariatric surgery.

NCT ID: NCT03150264 Recruiting - Clinical trials for Mechanical Ventilation

Prospective Clinical Study of PCV and PCV-VG in Patients Undergoing Bariatric Surgery

Start date: January 16, 2017
Phase: N/A
Study type: Interventional

This study compares the two mechanical ventilation strategies in obese patients undergoing bariatric surgery: pressure-controlled ventilation(PCV) and pressure-controlled ventilation volume-guaranteed(PCV-VG). This is a randomized controlled trial with a sample size of 100 patients whose body mass index(BMI) is over 30kg/m².

NCT ID: NCT03107702 Enrolling by invitation - POSTOPERATIVE PAIN Clinical Trials

Melatonin Level and Postoperative Analgesia Consumption in Bariatric Surgery Patients.

Start date: March 29, 2017
Phase: N/A
Study type: Observational

Bariatric surgical procedures are associated with low short-term mortality and may be associated with long-term reductions in all-cause, cardiovascular, and cancer-related mortality. This surgeries are major surgeries include risk of mortality still. Melatonin is a hormone secreted from the pineal gland. Melatonin is an antioxidant, antinociceptive, hypnotic, anticonvulsant, neuroprotective, anxiolytic, sedative and analgesic. Melatonin is neurohormone with the profile of a novel hypnotic-anesthetic agent. The purpose of this study is to investigate the preoperative, perioperative and postoperative melatonin levels in bariatric surgery under general anesthesia and to investigate the relationship between melatonin level and analgesia requirement.

NCT ID: NCT03049696 Active, not recruiting - Obesity Clinical Trials

Does Participation in a Pre-Operative Physical Activity Program Improve Patient Outcomes and Quality of Life?

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

The primary objective of the study is to determine whether participation in a pre-bariatric surgery physical activity and behavior modification/education program (ENCOURAGEING START) that is tailored to the unique needs of obese bariatric surgery patients, improves physical fitness, surgical outcomes, patient health and quality of life. Short- (one year) and long- (five year) term outcomes will be compared to matched historical controls (1:1) based on age, gender, and body mass index (BMI) from the existing Manitoba Centre for Metabolic and Bariatric Surgery (CMBS) database. Our findings will determine whether a pre-bariatric surgery physical activity and behavior modification/education program results in improve surgical and patient outcomes and inform the development of evidence-based physical activity (PA) guidelines for bariatric surgery patients and improved CMBS program delivery.

NCT ID: NCT03046186 Completed - Obesity, Morbid Clinical Trials

Physiological Effects of Gastric Sleeve Operation

Start date: June 2016
Phase:
Study type: Observational

After gastric sleeve patients undergo a substantial weight loss, but the physiological mechanisms behind the weight loss is not fully elucidated. Studies suggest that gut-hormone secretion is altered comparable to what is also seen after Roux-en-Y gastric bypass, however to which extent is not fully established and furthermore, the mechanisms behind an altered secretion are unclear. The purpose of this study is to investigate absorption and postprandial metabolism of glucose and protein in addition to gut hormonal responses after gastric sleeve compared with a group of un-operated subjects machted on sex, age and BMI. Furter, a group of Roux-en-Y gastric bypass operated patients matched on pre-operative BMI, current BMI, sex and age will be included for comparison.

NCT ID: NCT02973009 Withdrawn - Bariatric Surgery Clinical Trials

Impact of the Systematic Closure of the Epigastric Trocar on Postoperative Incisional Hernia After Sleeve Gastrectomy Rate of First Intention. Monocentric Study, Before / After Prospective.

TROCSLEEVE
Start date: May 16, 2017
Phase:
Study type: Observational

The Sleeve Gastrectomy (SG) is a bariatric surgery procedure performed by laparoscopic booming in recent years. This is an effective intervention on weight loss over the long term with few early postoperative complications and low morbidity in the long term. Obesity is considered as a risk factor for hernia full after surgery by laparoscopy with a relative risk of 29% in connection with cholecystectomy. Several series showed a rupture rate on trocar from 0 to 0.7%, but each time with a clinical evaluation. Recently, it was shown eventrations rate between 26 and 38% under the Roux-en-Y gastric bypass with a rupture rate increased on epigastric trocar. The assessment in the context of this series was ultrasound. Recent data suggest that the absence of closure of the epigastric trocar of 12mm through an SG of first intention was associated with a hernia rate of 17% with a scannographic evaluation. Also, recently, Tabone suggests that the systematic closure of the epigastric trocar site would not be as effective as lateralize inserting the trocar from the white line of the abdomen. Change the positioning of this trocar induce an additional difficulty in handling instruments for the realization of the SG with an désaxassion instruments, a conflict between the instruments for the realization of the SG and the optical laparoscopy.

NCT ID: NCT02857179 Recruiting - Bariatric Surgery Clinical Trials

Study of Bariatric Surgery

BARIASURG
Start date: November 2007
Phase: N/A
Study type: Observational

The aim of this cohort study is to collect prospectively clinical data on all the patients admitted in the investigators department for bariatric surgery or for any complication of a bariatric procedure. The investigators goal is not only to improve the follow-up but also to assess and publish the investigators results regarding weight loss and the complication rate.

NCT ID: NCT02817295 Completed - Bariatric Surgery Clinical Trials

Bariatric Surgeries in Elderly

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

an examination of the different aspects of bariatric surgery in elderly in comparison with non-elderly patients.

NCT ID: NCT02749305 Recruiting - Bariatric Surgery Clinical Trials

Comparative Effectiveness of Bariatric Surgery With PROMs

LOBSTER PROMs
Start date: March 2016
Phase: N/A
Study type: Interventional

This long-term, nationwide observational data collection repository will obtain patient-reported outcomes from metabolic and bariatric surgery patients. The data will be used in conjunction with clinical outcomes to determine quality, safety, and comparative effectiveness of various metabolic and bariatric procedures.