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Impact of opioid-free anesthesia on postoperative catheter-related bladder discomfort in elderly patients undergoing transurethral resection of bladder tumors: A single-center randomized controlled trial

Impact of opioid-free anesthesia on postoperative catheter-related bladder discomfort in elderly patients undergoing transurethral resection of bladder tumors: A single-center randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128748
Enrollment
Unknown
Registered
2026-07-24
Start date
2026-12-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

catheter-related bladder discomfort

Interventions

Test group :opioid-free anesthesia
Control group:opioid-based anesthesia

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 60 years; 2. A bladder tumor was confirmed via imaging studies (B-ultrasound, CT/MRI) or cystoscopic biopsy, transurethral resection of the bladder tumor (TURBT) is planned. 3. ASA grade ?-?; 4. Preoperative visual analog pain score (VAS) <=3 points; 5. Written informed consent was obtained from all participating patients.

Exclusion criteria

Exclusion criteria: 1. Allergic to the anesthetic agents used in the trial (e.g., propofol, dexmedetomidine, esketamine, rocuronium, etc.) or their excipients; 2. Preoperative moderate to severe pain (VAS> 3) or a history of long-term use of opioids or sedative-analgesic medications (>1 week); 3. Severe arrhythmias such as second-or third-degree atrioventricular block, sick sinus syndrome, or severe bradycardia (heart rate 180/100 mmHg); 5. Severe hepatic or renal dysfunction (e.g. Child-Pugh class C, or an estimated glomerular filtration rate <30 mL/min); 6. Severe cardiovascular diseases (e.g., heart failure, unstable angina); respiratory diseases (e.g., acute exacerbation of chronic obstructive pulmonary disease, respiratory failure); 7. Mental disorders, cognitive dysfunction, or communication impairments; 8. participation in other clinical trials within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Incidence of CRBD within 24 hours postoperatively;

Secondary

MeasureTime frame
postoperative sedation levels;Intraoperative HR;CRBD severity at 0,1h,2h,6h and 24h postoperatively;the use of vasoactive drugs during the operation;Extubation time;postoperative duration of urinary catheter placement;Occurrence of postoperative adverse events;pain scores at rest at 0,1h,2h,6h and 24h postoperatively;postoperative hospital stays;Intraoperative MAP;Use of analgesics and M-receptor blockers within 24 hours postoperatively;the 15-item quality of recovery (QoR-15) score at 24hour after surgery;eye opening time;time to shift to PACU;PACU stay time;Incidence of CRBD at 0,1h,2h,6h and 24h postoperatively;pain scores during movement at 0,1h,2h,6h and 24h postoperatively;

Countries

China

Contacts

Public ContactXueyuan Yang

Peking University First Hospital

yxy8121@163.com+86 10 83575138

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026