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Effects of Sugammadex Sodium on Postoperative Neuromuscular Recovery and Pulmonary Complications in Elderly Patients Undergoing Transurethral Resection of Bladder Tumor: A Double-blind Randomized Controlled Trial

Effects of Sugammadex Sodium on Postoperative Neuromuscular Recovery and Pulmonary Complications in Elderly Patients Undergoing Transurethral Resection of Bladder Tumor: A Double-blind Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112148
Enrollment
Unknown
Registered
2025-11-11
Start date
2025-11-24
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Bladder tumour

Interventions

Sugammadex group (S group):After surgery, administer sugammadex 2 mg/kg intravenously when the third twitch (T3) appears during the train-of-four (TOF) stimulation, and remove the laryngeal mask when
Neostigmine group (N group):After surgery, administer neostigmine 0.05 mg/kg intravenously (maximum dose 5 mg) + atropine 0.02 mg/kg when the third twitch (T3) appears during the train-of-four (TOF) s

Sponsors

Anqing Municipal Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective transurethral resection of bladder tumor; 2. ASA classification I-III; 3. Age 60-80 years; 4. BMI 18-32 kg/m^2, and weight >40 kg; 5. Ethical compliance, patients voluntarily agree to participate in this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Severe impairment of heart, lung, liver, and kidney function; 2.History of mental illness or long-term use of psychotropic medications (e.g., dementia, schizophrenia), chronic analgesic use, myasthenia gravis, or alcohol abuse; 3.Patients with severe infection; 4.Patients with language, hearing impairments, or brain dysfunction (e.g., stroke) that prevent communication; 5.Preoperative PaO2<60 mmHg or SpO2<92%; 6.Participation in another drug clinical trial within the past 30 days.

Design outcomes

Primary

MeasureTime frame
Postoperative pulmonary complication rate;

Secondary

MeasureTime frame
postoperative muscle relaxation recovery effect;Hemodynamic indicators;Quality of recovery on the first postoperative day (Q-15 score scale);incidence of postoperative adverse events ;30-day postoperative readmission rate;length of hospital stay;

Countries

China

Contacts

Public ContactDuan Jinjuan

Anqing Municipal Hospital

djjayd223@163.com+86 189 0966 5698

Outcome results

None listed

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