Comparative study of analgesia by the use of intravenous and subarachnoid clonidine in patients submitted to Videoolaparoscopic Cholecystectomy
- Conditions
- Cholelithiasis.C06.130.409
- Registration Number
- RBR-33vyhm
- Lead Sponsor
- Fundação Universidade do Amazonas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Voluntary patients; of both sexes; with full autonomy; ages ranging from 18 to 50 years; weight between 50 and 100 kg; with diagnosis of cholelithiasis; classification I or II of the physical state according to the scale of the American Society of Anesthesiologists.
Patients who refuse to sign the informed consent form (EHIC); withdrawals; pregnant or nursing mothers; indigenous peoples; minor or legally incapable; patients with special needs; patients on uninterrupted use of analgesics; with a history of hypersensitivity to any of the medications used in the procedure; patients diagnosed with depression; patients with liver disease, nephropathy or with blood coagulation disorders; conversion of videolaparoscopic surgery in conventional open surgery.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method