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Comparison of the Efficacy and Safety of Propofol Combined with Remifentanil, Esketamine, or Oxycodone MAC Regimens in Transperineal Prostate Biopsy

Comparison of the Efficacy and Safety of Propofol Combined with Remifentanil, Esketamine, or Oxycodone MAC Regimens in Transperineal Prostate Biopsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113722
Enrollment
Unknown
Registered
2025-12-02
Start date
2026-03-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Painless prostate biopsy

Interventions

R group:Propofol and Remifentanil
E group:Propofol and Esketamine
O group:Propofol and Ozelidine

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for transperineal prostate biopsy; 2. Age 18–85 years; 3. Body Mass Index (BMI) 18–30 kg/m^2 ; 4. American Society of Anesthesiologists (ASA) classification I–III; 5. Preoperative assessment indicates no difficult airway.

Exclusion criteria

Exclusion criteria: 1. History of severe heart, brain, lung, liver, kidney, or metabolic diseases; 2. Patients with gastrointestinal obstruction; 3. History of acute respiratory inflammation within the past 2 weeks that has not been cured; 4. Individuals with neuromuscular system disorders or mental illnesses; 5. Suspected abuse of narcotic analgesics or sedatives; 6. Predicted or previous occurrence of difficult airway; 7. Known allergy to remifentanil, esketamine, or oliceridine; 8. Concurrent use of other sedative or analgesic drugs within 15 minutes before, during, or after surgery (including injections, oral medications, and related traditional Chinese medicine preparations); 9. Individuals who are uncooperative or unable to communicate

Design outcomes

Primary

MeasureTime frame
Incidence of respiratory depression;

Secondary

MeasureTime frame
Patient and operator satisfaction;Administer an additional dose of propofol;Degree of respiratory depression;Loop parameter;Adverse reaction;Does body movement affect the operation?;Wake-up time;Surgery time;

Countries

China

Contacts

Public ContactYi Zhou

Shanghai Changhai Hospital

Yizhoumz@163.com+86 137 6129 3168

Outcome results

None listed

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