Skip to content

Effects of Esketamine Combined with Ropivacaine for Transversus Abdominis Plane Block on Postoperative CRBD and Pain in Patients Undergoing Prostate Cancer Surgery

Effects of Esketamine Combined with Ropivacaine for Transversus Abdominis Plane Block on Postoperative CRBD and Pain in Patients Undergoing Prostate Cancer Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124008
Enrollment
Unknown
Registered
2026-05-06
Start date
2025-02-03
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Prostate Cancer

Interventions

Ropivacaine TFPB Group (T Group):0.3% Ropivacaine 25mL injected into the transversus abdominis plane
Esmirtamine Combined with Ropivacaine TFPB Group (ET Group):0.3% Ropivacaine combined with 0.2mg/kg Esmirtamine, total 25mL injected into the transversus abdominis plane
Control Group (C Group):0.9% Normal Saline 25mL injected into the transversus abdominis plane

Sponsors

Ningbo Medical Center Li Huili Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for laparoscopic radical prostatectomy; 2. Male, aged 60 to 85; 3. American Society of Anesthesiologists (ASA) classification I-III; 4. No abnormal coagulation function; 5. No neurogenic bladder; 6. No research on drug allergy. 7. Subjects who agreed to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Severe visual and hearing disorders; 2. Those who are unable to cooperate to complete the test; 3. Serious diseases of the heart, brain, lungs, liver and kidneys; 4. History of drug abuse or addiction; 5. There were mental disorders and cognitive impairments before the operation; 6. History of local anesthetic allergy; 7. Infection at the puncture site. 1) Occurrence of serious adverse events during the perioperative period (massive hemorrhage, deterioration of underlying diseases, and postoperative admission to the ICU, etc.); 2) The TFPB operation failed.

Design outcomes

Primary

MeasureTime frame
Incidence and grading of CRBD and visual analog scale (VAS) pain scores at multiple time points within 24 hours postoperatively;

Secondary

MeasureTime frame
Incidence and grading of CRBD;Opioid consumption;Number of patient-controlled analgesia (PCA) uses and rescue analgesia requirements postoperatively;Early postoperative enhanced recovery after surgery (ERAS) related indicators;

Countries

China

Contacts

Public ContactXu Wenfei

Ningbo Medical Center Li Huili Hospital

281592520@qq.com+86 136 8570 7452

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026