Anesthesia Recovery Clinical Trial
Official title:
"Low Dose Sugammadex Combined With Neostigmine and Glycopyrrolate Versus Full Dose Sugammadex for Reversal of Rocuronium-induced Neuromuscular Blockade: a Cost Saving Strategy"
Verified date | June 2018 |
Source | American University of Beirut Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Prospective Randomized non inferiority Trial involving adult patients undergoing elective surgery under general anesthesia.56 Patients will be enrolled in 2 groups : full dose sugammadex vs half dose sugammadex for reversal of NMB.
Status | Completed |
Enrollment | 56 |
Est. completion date | October 2015 |
Est. primary completion date | October 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Patients aged 18-70 - ASA class I, II, and III - undergoing surgery under balanced general anesthesia requiring the use of muscle relaxants throughout the surgery Exclusion Criteria: - patients undergoing emergency surgeries - pregnant patients - patients with end stage renal disease or chronic kidney disease(GFR less than 60) - patients with allergy to sugammadex or who had previous complications or side effects from previous sugammadex administration - patients' refusal - patients with allergy to recuronium |
Country | Name | City | State |
---|---|---|---|
Lebanon | AUBMC | Beirut |
Lead Sponsor | Collaborator |
---|---|
American University of Beirut Medical Center |
Lebanon,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | TOF ratio of 0.9 | within 5 minutes | ||
Secondary | the time to return of TOF ratio to 0.9 and the time till extubation | within 10 minutes | ||
Secondary | Residual neuro-muscular blockade | Post Anesthesia recovery unit | within 10 to 180 mins |
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