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A Study of the Effect of Intravenous Rocuronium Bromide on Neuromonitoring and Surgical Satisfaction in Thyroid Surgery

A Study of the Effect of Intravenous Rocuronium Bromide on Neuromonitoring and Surgical Satisfaction in Thyroid Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110530
Enrollment
Unknown
Registered
2025-10-15
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Thyroid cancer

Interventions

R1 group:Continuous intraoperative infusion of rocuronium bromide (3~5µg/kg/min)
R2 group:Intermittent intravenous injection of 1/5 of the induction dose
R3 group:Intermittent intravenous injection of 1/6 of the induction dose

Sponsors

Luwan Branch of Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients aged 18-50 years with ASA classification I-II undergoing radical thyroidectomy

Exclusion criteria

Exclusion criteria: 1. Patients with a history of neuromuscular diseases; 2. Those with a previous recurrent laryngeal nerve injury or vocal cord paralysis; 3. Patients with preoperative liver or kidney dysfunction; 4. Patients identified as allergic to rocuronium bromide; 5. Patients with peripheral neuromuscular disease, a history of forearm or distal limb surgery, or those for whom neuromuscular monitoring cannot be performed.

Design outcomes

Primary

MeasureTime frame
Intraoperative satisfaction score;

Secondary

MeasureTime frame
Differences in success rates of neural monitoring;Differences in amplitude of neural stimulation signals;Differences in postoperative extubation time and adverse reactions during the recovery period;

Countries

China

Contacts

Public ContactShen Liang

Luwan Branch of Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

Shenliang701110@163.com+86 137 0180 3747

Outcome results

None listed

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