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Incidence of Postoperative Residual Neuromuscular Blockade in the Era of Sugammadex

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Seoul National University

Status

Enrolling

Conditions

Postoperative Residual Curarization

Treatments

Drug: Sugammadex

Study type

Observational

Funder types

Other

Identifiers

NCT05760560
TOF-Sugammadex

Details and patient eligibility

About

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.

Enrollment

52 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Central trial contact

Chang-Hoon Koo

Data sourced from clinicaltrials.gov

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