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Comparison of Oxycodone and Sufentanil for Preventing Catheter-Related Bladder Discomfort After Transurethral Resection of the Prostate: A Randomized, Double-Blind, Parallel-Group Controlled Trial

Comparison of Oxycodone and Sufentanil for Preventing Catheter-Related Bladder Discomfort After Transurethral Resection of the Prostate: A Randomized, Double-Blind, Parallel-Group Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126594
Enrollment
Unknown
Registered
2026-06-11
Start date
2026-06-15
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Benign Prostatic Hyperplasia

Interventions

Oxycodone group:Oxycodone was used as the opioid for both anesthesia induction and maintenance
Sufentanil group:Sufentanil was used as the opioid for both anesthesia induction and maintenance

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Male patients scheduled for elective transurethral resection of the prostate (TURP) or holmium laser enucleation of the prostate (HoLEP) under general anesthesia; 2.Aged 50–75 years; 3.Body mass index (BMI) between 18 and 28 kg/m2; 4.American Society of Anesthesiologists (ASA) physical status classification I or II; 5.Postoperative indwelling of a F20 three-way urinary catheter;

Exclusion criteria

Exclusion criteria: 1.Allergy to oxycodone or sufentanil; 2.Use of anticholinergics, antihistamines, or sedatives within 24 hours before surgery; 3.Severe cardiovascular or respiratory disease, or hepatic or renal dysfunction; 4.History of chronic pain or long-term opioid use; 5.Concomitant neurological diseases affecting bladder function or sensation (e.g., multiple sclerosis, spinal cord injury); 6.Pre-existing overactive bladder, neurogenic bladder, or acute/chronic urinary tract infection before surgery; 7.Previous penile or prostate surgery; 8.History of urinary catheterization or indwelling catheter within the past 3 months; 9.Expected surgery duration 2 hours, or anticipated conversion to open surgery; 10.Refusal to participate in the study;

Design outcomes

Primary

MeasureTime frame
Incidence of moderate-to-severe CRBD within 6 hours postoperatively;

Secondary

MeasureTime frame
Analgesic rescue treatment;Rescue treatment for CRBD;Other adverse events;Excessive sedation;Incidence of moderate-to-severe CRBD at each time point;Emergence agitation;Overall incidence of CRBD at each time point;Respiratory depression;Postoperative pain severity;Patient satisfaction score;Postoperative nausea and vomiting;CRBD Severity Score;

Countries

China

Contacts

Public ContactWang Liangrong

The First Affiliated Hospital of Wenzhou Medical University

arerong@163.com+86 135 8788 4540

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026