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Postoperative analgesic effects of combined transversus abdominis plane block and anterior approach of sacral plexus block in patients undergoing laparoscopic radical prostatectomy: a randomized controlled trial

Postoperative analgesic effects of combined transversus abdominis plane block and anterior approach of sacral plexus block in patients undergoing laparoscopic radical prostatectomy: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076374
Enrollment
Unknown
Registered
2023-10-07
Start date
2023-10-09
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

regional block

Interventions

Experimental group 1:transversus abdominis plane block
Experimental group 2:transversus abdominis plane block combined with anterior approach for sacral plexus block

Sponsors

Beijing Chaoyang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.age 40-80 years;2.BMI < 30kg/m2;3.ASA I-III;4.Patients undergoing laparoscopic radical prostatectomy;5.Patiens who were aware of the study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with puncture site infection;2.Patients with coagulation disorders;3.Patients allergic to local anesthetics;4.Patients with severe cardiovascular and pulmonary disease;5.Patients with hepatic and renal dysfunction;6.Patients with nervous system disease;7.Patients with chronic opioid use;8.Patients who converted to open surgery ;9. Patients with previous prostate or bladder surgery;10. Patients using the anticholinergic drug

Design outcomes

Primary

MeasureTime frame
consumption of total intravenous morphine equivalent within the first 24 h after surgery;

Secondary

MeasureTime frame
consumption of intravenous morphine equivalent during 0-12h?12-24h?24-48h after surgery;resting NRS pain score at 1h?4h?8h?12h?24h after surgery;NRS pain score during coughing at 1h?4h?8h?12h?24h after surgery;need for rescue analgesic within 24h after surgery;time to first PCA press;QoR-15 score at 48h after surgery;time to first ambulation;incidence of postoperative side effects within 48 h after surgery.;time to first flatus;length of stay;patient satisfaction with analgesic approach;classification of the severity of catheter-related bladder discomfort at 1h?4h?8h?12h?24h after surgery;

Countries

China

Contacts

Public ContactYun Wang

Beijing Chaoyang Hospital, Capital Medical University

wangyun129@ccmu.edu.cn+86 135 2161 1825

Outcome results

None listed

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