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Randomized controlled trial of sugammadex or neostigmine on postoperative pulmonary complications in elderly patients undergoing urologic surgery

Randomized controlled trial of sugammadex or neostigmine for reversal of neuromuscular block on the incidence of postoperative pulmonary complications in elderly patients undergoing urologic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0005630
Enrollment
180
Registered
2020-11-24
Start date
2020-11-18
Completion date
Unknown
Last updated
2020-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : At the end of the surgery, when the Train-of-four counts is 2 or more, the anesthesiologist will administer sugammadex (experimental group) 2mg/kg or neostigmine (control group) 0.07mg/kg (maxi

Sponsors

Ajou University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Patients undergoing general anesthesia for transurethral resection of prostate or bladder tumor - American Society of Anesthesiologists (ASA) physical status I-III

Exclusion criteria

Exclusion criteria: - Severe chronic renal disease - Severe chronic liver disease - Allergy to sugammadex or neostigmine - Pregnancy - Patients who lack decision-making ability

Design outcomes

Primary

MeasureTime frame
Total incidence of postoperative pulmonary complications

Secondary

MeasureTime frame
The incidence of residual neuromuscular block;Time taken to extubation after administation of reverse agents;Time taken to exit the operating room after administation of reverse agents;Time spent in the postanesthesia care unit;The incidence of postoperative complications;The length of hospital stay;Readmission within 30 days after surgery

Countries

Korea, Republic of

Contacts

Public ContactMin Hur

Ajou University Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026