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Comparison of postoperative pain between low pressure pneumoperitoneum and standard pressure pneumoperitoneum in robotic-assisted laparoscopic radical prostatectomy : a randomized control trial

Comparison of postoperative pain between low pressure pneumoperitoneum and standard pressure pneumoperitoneum in robotic-assisted laparoscopic radical prostatectomy : a randomized control trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240601002
Enrollment
100
Registered
2024-06-01
Start date
2024-03-26
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Post operative pain of Patients with Prostate cancer that underwent Robotic-assisted Radical Prostatectomy Prostate cancer, Robotic-assisted radical prostatectomy, Pneumoperitoneum, Robotic surgery, Postoperative pain, Urological surgery

Interventions

Using Pneumoperitoneum pressure of 8 mmHg during Robotic-assisted Radical Prostatectomy,Using Pneumoperitoneum pressure of 12 mmHg during Robotic-assisted Radical Prostatectomy
Experimental Procedure/Surgery,No Intervention Procedure/Surgery
Pneumoperitoneum pressure 8 mmHg,Pneumoperitoneum pressure 12 mmHg

Sponsors

Faculty of Medicine Ramathibodi Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients were diagnosed with pathologically proven prostate cancer 2.Male age > 18 year-old 3.Patients must be cognitively intact, and fully able to understand and answer question by himself 4.Patients will undergo Robotic-assisted Radical Prostatectomy by Prof. Kittinut Kijvikai and Assistant Prof. Wattanachai Ratanasompong

Exclusion criteria

Exclusion criteria: 1.Prostate cancer patients who have been treated with radiotherapy or brachytherapy 2.Patients who have advanced prostate cancer with metastases to other organs except the lymph nodes

Design outcomes

Primary

MeasureTime frame
Postoperative pain 4 hr, 12 hr, 24 hr, and 48 hr Post op. Numerical rating pain scale

Secondary

MeasureTime frame
Dosage of opoid use 48 hour post op. mg,Postoperative prolonged bowel ileus 48 hour post op. Yes/No,Length of hospital stay Unitl the patient is discharged home Days,Operative Console time Intraoperatively minutes,Surgical margin status Postoperatively Positive/Negative according to the pathological report

Countries

Thailand

Contacts

Public ContactManapol Rujithamkul

Faculty of Medicine Ramathibodi Hospital

manapol_22@hotmail.com0898935105

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026