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The comparison of different sugammadex administration on the total doseage and postoperative residual neuromuscular blockade in elderly patients with sarcopenia

The comparison of different sugammadex administration on the total doseage and postoperative residual neuromuscular blockade in elderly patients with sarcopenia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091593
Enrollment
Unknown
Registered
2024-10-30
Start date
2024-10-31
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

Sarcopenia

Interventions

Control group:Single administration
Experimental group:Titration administration

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age = 65 years; (2) ASA classification 1 to 3; (3) Undergoing elective or semi-elective abdominal surgery; (4) Diagnostic criteria for sarcopenia: L3-SMI: < 50 cm²/m² for males, < 39 cm²/m² for females.

Exclusion criteria

Exclusion criteria: (1) Allergy to sugammadex (SUG); (2) Use of medications that affect the metabolism of neuromuscular blocking agents, such as valproate, carbamazepine, phenytoin, quinidine, calcium channel blockers, magnesium, aminoglycoside antibiotics, etc.; (3) Patients unable to undergo neuromuscular monitoring, such as those with central or peripheral neuromuscular diseases; (4) Renal dysfunction: Estimated Glomerular Filtration Rate (eGFR) < 60 ml/min; (5) No severe comorbidities involving major organs such as the heart, lungs, or liver. Cardiac diseases include but are not limited to coronary artery disease, myocardial infarction, heart failure, etc.; pulmonary diseases include but are not limited to chronic obstructive pulmonary disease, pulmonary embolism, severe asthma, etc.; liver diseases include but are not limited to cirrhosis, severe liver insufficiency, liver tumors, etc.

Design outcomes

Primary

MeasureTime frame
Total SUG dose (mg/kg) required for TOFr to recover to =0.9;

Secondary

MeasureTime frame
Time required for TOFr to recover to =0.9;Incidence of postoperative residual neuromuscular blockade (TOFr =0.9 followed by <0.9);Spontaneous recovery rate of TOFr before SUG administration (?TOFr/min);Administration responsiveness: recovery rate of TOFr (?TOFr/min) after administration of SUG, including early recovery rate and late recovery rate;Postoperative PACU recovery, including time to extubation, time to PACU discharge from the operating room;Incidence of postoperative pulmonary complications, e.g., pneumonia, hypoxemia, re- intubation, ventilator support therapy, respiratory failure;Early postoperative recovery: includes the Quality of Recovery Rating Scale-15 (QoR-15) to assess the quality of the patient's early postoperative recovery, time to the first out-of-bed activity, days of hospitalization, and rate of rehospitalization within 7 days;

Countries

China

Contacts

Public ContactQIONG YU

Huashan Hospital, Fudan University

yu_qiong816@sina.com+86 134 7275 5168

Outcome results

None listed

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