Anesthesia Clinical Trial
Official title:
Multimodal Opioid-free Anesthesia Versus Opioid-based Anesthesia for Patients Undergoing Cardiac Valve Surgeries: A Randomized Controlled Trial
Verified date | August 2023 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Several studies demonstrated the effectiveness of OFA in patients undergoing non-cardiac surgery. Preoperative use of Cox inhibitors, GABA analogues and acetaminophen have been shown to decrease use of opioids postoperatively . Intraoperative use of agents that lead to opioid sparing effects via sodium channel blockade, blockade of G protein-coupled receptors, NMDA blockade, central alpha-2 agonists and anti-inflammatory effects can make opioid-free anesthesia (OFA) possible. On the other hand, there have been no studies demonstrating the effectiveness of an OFA technique in patients undergoing cardiac surgery except for two case reports who successfully implemented the OFA regimen in two patients undergoing valve replacement surgeries. The investigators therefore propose this prospective randomized controlled trial to investigate whether a multimodal opioid-free anesthesia regimen will be suitable as an alternative to conventional opioid-based regimen in patients undergoing valve surgery
Status | Completed |
Enrollment | 60 |
Est. completion date | October 1, 2022 |
Est. primary completion date | August 1, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: 1. Patients undergoing cardiac valve surgeries ( replacement or repair ) . 2. Age (18-80) years 3. Both sexes Exclusion Criteria: - Patient refusal - Known allergy to any of the medications used in the study - Combined valve and CABG surgeries - Redo surgery - Infective endocarditis - Patients in heart failure or heart block or with significant systolic dysfunction (EF < 40%) or diastolic dysfunction more than grade II - Pregnant females - Patients being treated for chronic pain or with recent use (< two weeks) of opioids, gabapentin, or pregabalin. - Substance abuse - Patients with renal impairment (creatinine > 2 mg/dL) or hepatic impairment (ALT > 2 folds, INR > 1.5 and/or serum albumin < 2.5 g/dl) |
Country | Name | City | State |
---|---|---|---|
Egypt | Kasr Al Ainy School of Medicine Cairo University | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Extubation time (min) | Extubation time, defined as the time from discontinuation of inhalation agents to extubation | 24 hours | |
Secondary | Heart rate (beats/min) | HR
o Arterial blood pressure (systolic, diastolic, and mean) |
24 hours | |
Secondary | Blood pressure (mm Hg) | Systolic, diastolic, and mean blood pressure | 24 hours | |
Secondary | Postoperative rescue analgesia (number) | The number of patients requiring rescue analgesia with Morphine | 24 | |
Secondary | Postoperative morphine consumption (mg) | The total dose of morphine administered | 24 hours |
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