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Effect of Oliceridine vs. Sufentanil in Intravenous Analgesia Pumps after Urethral Surgery on Postoperative Acute and Chronic Pain, and Incidence of Early Moderate-to-Severe Postoperative Pain: A Randomized and Controlled Clinical Trial

Feasibility, Efficacy and Safety of Oliceridine in Perioperative Analgesia for Patients with Posterior Urethral Stricture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108926
Enrollment
Unknown
Registered
2025-09-09
Start date
2025-10-16
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Urethral stricture

Interventions

Sponsors

Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male patients scheduled for a urethral surgery under general anesthesia; 2. Age ranging from 18 to 65 years old; 3. ASA classification grade I to III; 4. BMI ranging from 18 to 30 kg/m^2; 5. Voluntary use of postoperative intravenous analgesic pump; 6. Patients or authorized family members have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. There are contraindications for using oliceridine (such as severe respiratory depression, paralytic intestinal obstruction, and allergy to oliceridine); 2. The surgical site was painful before the operation; 3. Long-term use of psychotropic drugs or opioid drugs; 4. Severe impairment of heart, lung, liver, and kidney functions; 5. Allergic to other drugs involved in this study; 6. Difficult cooperation, intellectual disability, or cognitive dysfunction before the operation; 7. Has participated in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Pain score;

Secondary

MeasureTime frame
Postoperative nausea and vomiting;Postoperative respiratory depression;Postoperative drowsiness;Sleep disturbance;The time of the first rescue analgesia after surgery and the number of rescue analgesia administrations;The time of the first postoperative ambulation;EuroQol Five-Dimensional Scale Score;inflammatory factor;Anxiety and depression scores;postoperative moderate to severe acute pain;Blood test indicators;Additional adverse reactions;

Countries

China

Contacts

Public ContactYushan Dong

Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

practitioner_dys@foxmail.com+86 139 5630 9323

Outcome results

None listed

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