Bariatric Surgery (Sleeve Gastrectomy )

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Review clinical trials related to Bariatric Surgery (Sleeve Gastrectomy ). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Identification of Pre-surgical Phenotypic Indicators Predictive of Quality of Life Trajectories in Obese Patients Following Bariatric Surgery

This study aims to identify pre-operative phenotypic determinants predictive of quality of life trajectories in post-bariatric surgery patients. In addition, this study will have as a secondary objective the highlighting of a potential link between post-surgery quality of life trajectories and those of anxiety/depression scores, eating behaviors and body mass indices. This study will be conducted during the usual care of patients undergoing the GEROM73 program, lasting a total of 30 months. The GEROM73 program includes care for the six months preceding bariatric surgery and the 24 months following surgery. This program supports patients throughout their bariatric care.. Throughout the GEROM73 program, patients will complete questionnaires on anxiety, depression, eating disorders, Impact of Weight on Quality Of Life. Patients' weight, body mass index and body schema will also be measured throughout the GEROM program.

Participants needed: 165
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Metropole SavoieUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

patient > 18years old [+1]

Patients in a state of psychiatric decompensation [+3]

Status: Recruiting

Flow-Controlled vs Volume-Controlled Ventilation in Morbidly Obese Patients Undergoing Laparoscopic Bariatric Surgery

The goal of this clinical trial is to compare the effects of flow-controlled ventilation (FCV) and volume-controlled ventilation (VCV) on hemodynamic and respiratory parameters in obese patients undergoing elective laparoscopic bariatric surgery. The main questions it aims to answer are: Does FCV provide better intraoperative hemodynamic and respiratory stability compared to VCV during laparoscopic bariatric surgery? Is FCV a safe and feasible ventilation strategy under high intraabdominal pressure and position changes required in bariatric surgery? Researchers will compare FCV group to VCV group to see if FCV improves intraoperative respiratory mechanics and hemodynamic parameters. Participants will: Undergo elective laparoscopic bariatric surgery with BMI \>40 kg/m² (ASA I-III) Receive either flow-controlled or volume-controlled ventilation with individualized PEEP and tidal volume of 6-8 ml/kg predicted body weight Have intraoperative hemodynamic and respiratory parameters monitored at regular intervals, including arterial blood gas analysis Be followed postoperatively for oxygen therapy requirement and intensive care need

Participants needed: 34
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ankara Training and Research HospitalUpdated: Jun 11, 2026Locations: 1
Eligibility criteria

Age between 18 and 65 years American Society of Anesthesiologists (ASA) physical...

ASA physical status IV or V Emergency surgical procedures Pregnant patients Pati...

Status: Recruiting

The Effect of Tele-Counseling Service on Nutrition, Exercise Attitude, and Medication Adherence After Bariatric Surgery

The aim of this study was to evaluate the effects of teleconsultation service on nutrition, exercise attitudes and medication adherence after bariatric surgery.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Cukurova UniversityUpdated: Sep 3, 2025Locations: 1
Eligibility criteria

Patients who have undergone laparoscopic bariatric surgery (sleeve gastrectomy o... [+5]

Patients who developed early postoperative complications (bleeding, anastomotic...

Status: Recruiting

Establishment of a Classification System and Postoperative Risk Warning Model for Patients Undergoing Bariatric Metabolic Surgery for Severe Obesity

This study aims to establish a classification system for patients undergoing metabolic surgery for severe obesity by constructing a prospective cohort of 2,000 patients and collecting clinical and biological data at multiple time points before and after surgery. By analyzing clinical, laboratory, and multi-omics characteristics, the study will identify indicators associated with postoperative adverse events and develop a risk warning model using machine learning algorithms. Ultimately, an intelligent digital system will be developed based on the classification criteria and risk model, integrating surgical classification and risk alert functions to provide real-time feedback, supporting clinicians and patients in optimizing postoperative treatment and risk management.

Participants needed: 2,000
Trial details
Age: 18-50Biological sex: AllType: ObservationalSponsor: The Third Xiangya Hospital of Central South UniversityUpdated: Jul 30, 2025Locations: 1
Eligibility criteria

Patients who meet the clinical indications for bariatric/metabolic surgery; [+1]

① Patients with conditions affecting the immune or metabolic systems (e.g., endo... [+4]

Status: Not yet recruiting

Non-opioid Anesthesia Based on Thoracic Paravertebral Block During Laparoscopic Sleeve Gastrectomy

Regional anesthesia is a technique in which a local anesthetic is injected near a nerve or spinal cord to block sensation, motor stimulation, and pain. In this study, an ultrasound-guided paravertebral block will be used, with careful consideration of all positive and negative factors and possible complications. A thoracic paravertebral block is performed by inserting a needle into the intercostal spaces on the back, approximately 4 cm lateral to the spine. Many studies support excellent pain control with this technique, during and after surgery in thoracic and abdominal surgery. Investigators aim to achieve faster patient mobility after surgery, rapid recovery of bowel function, reduced nausea and vomiting, and maximum pain control. The use of opioids, which can additionally cause respiratory suppression and drowsiness, is avoided. At any time in case of need to switch from laparoscopic to open surgery, equally adequate anesthesia and postoperative analgesia are ensured without the need to change the approach to the same. In this study, the basic scientific assumption (hypothesis) of the researchers is that non-opioid anesthesia with thoracic paravertebral block provides adequate pain control during and long-term after the surgical procedure, without the side effects of opioid anesthesia. The main goal of the study is to determine which type of anesthesia results in the best pain control and most significantly reduces complications of anesthesia and surgery in overweight patients who are scheduled for laparoscopic longitudinal gastrectomy and partial/total gastrectomy.

Participants needed: 36
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: IVO JURISICUpdated: Jul 24, 2025Locations: 1
Eligibility criteria

body mass index of 30 kg/m² or greater [+1]

allergies to the intended medications [+9]