Skip to content

Comparison between the effects of deep and moderate neuromuscular blockade during RFCA(Radiofrequency catheter ablation) on procedure condition and outcomes: a prospective, randomized, and controlled trial

Comparison between the effects of deep and moderate neuromuscular blockade during RFCA(Radiofrequency catheter ablation) on procedure condition and outcomes: a prospective, randomized, and controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0003371
Enrollment
96
Registered
2018-11-23
Start date
2019-02-14
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

None listed

Interventions

Drug : In group M, initiate the initial continuous infusion dose at 5 mcg / kg / min and maintain TOF1-2 under TOF monitoring. Reduce by 0.5 mg for TOF 0 and increase by 0.5 mg for TOF 3-4. In group D

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult patients with ASA class I-IV (aged 19-70 years) 2) Patients diagnosed with atrial fibrillation and underwent RFCA for the first time under general anesthesia

Exclusion criteria

Exclusion criteria: 1) Children (under 19 years old) 2) Patients who were diagnosed with atrial fibrillation and underwent RFCA 3) Patients with a high likelihood of lung aspiration 4) Patient with unstable vital signs 5) Patients with liver, kidney disease 6) Patients with metabolic diseases 7) Emergency surgery 8) Pregnant women,

Design outcomes

Primary

MeasureTime frame
Recurrence rate according to degree of muscle relaxation

Secondary

MeasureTime frame
Continuous variable: Heart Rate, Blood Pressure, Bispectral index(BIS);operation time;Self respiration recovery number of times;Operator satisfaction score

Countries

Korea, Republic of

Contacts

Public ContactJin hee Ahn

Samsung Medical Center

blattblatt@naver.com+82-2-3410-2470

Outcome results

None listed

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