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Incidence of Postoperative Residual Neuromuscular Blockade in the Era of Sugammadex

Incidence of Postoperative Residual Neuromuscular Blockade in the Era of Sugammadex

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05760560
Enrollment
52
Registered
2023-03-08
Start date
2023-03-15
Completion date
2024-08-31
Last updated
2023-04-14

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

Conditions

Postoperative Residual Curarization

Brief summary

This study is a prospective observational study. A total 52 patients will be included in this study. We will observe the incidence of postoperative residual neuromuscular blockade in patients receiving sugammadex.

Interventions

DRUGSugammadex

At the end of surgery, neuromucular blockade will be reversed with 2mg/kg or 4mg/kg sugammadex depending on the depth of neuromuscular blockade.

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients undergoing elective surgery under general anesthesia. * American Society of Anesthesiologists grade 1, 2, or 3. * Aged \>18 years

Exclusion criteria

* Refusal to participate in the study * Body Mass Index \< 18.5 kg/m2 or \> 35 kg/m2 * History of neuromuscular disease. * History of allergy to neuromuscular blockade * Scheduled to transfer to the intensive care unit

Design outcomes

Primary

MeasureTime frameDescription
Postoperative residual neuromuscular blockadeOn the arrival of PACUTOF ratio \< 0.9

Countries

South Korea

Contacts

Primary ContactChang-Hoon Koo
vollock9@gmail.com+821085098841

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026