The effect of the depth of neuromuscular block and pneumoperitoneum on postoperative pain after a gastric bypass
Not yet recruiting
- Conditions
- EN: Morbid obesity, bariatric surgery, gastric bypass, postoperative pain, pneumoperitoneum, deep neuromuscular blockNL: Morbide obesitas, bariatrische chirurgie, gastric bypass, postoperatieve pijn, pneunoperitoneum, diepe neuromusculaire block.
- Registration Number
- NL-OMON26521
- Lead Sponsor
- Franciscus Gasthuis & Vlietland
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Primary bariatric procedure; good command of the Dutch language.
Exclusion Criteria
Allergies for used medication, neuromuscular comorbidities, a medical history of pain disorders such as ACNES, fibromyalgia or CRPS, insufficient command of the Dutch language or unwillingness to supply informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of the pilot study is to determine which of the 4 groups are feasible to include in the actual trial. A cut off point of conversion from one of the treatment arms of more than 40% of the patients has been set to determine if that treatment arm is feasible to include in the trial.
- Secondary Outcome Measures
Name Time Method Secondary outcome measures are postoperative pain.