Impact of multimodal analgesic bundle on early postoperatvie pain in patients undergoing robot-assisted laparoscopic prostatectomy

Recruiting

• Conditions: Diseases of The genitoruinary system

• Registration Number: KCT0005376
• Lead Sponsor: The Catholic University of Korea, Seoul St. Mary's Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 September 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Male
• Target Recruitment: 80

Inclusion Criteria

1. Robotic-assisted laparoscopic prostate cancer surgery at Seoul St. Mary's Hospital
2. Adults (age more than 19 years old and less than 75 years old)
3. American Society of Anesthesiologists grade 1 or 2

Exclusion Criteria

1. Disagreement to participate in this study
2. Contraindication to rectus sheath block
3. Children (less than 19 years old)
4. Old (more than 75 years old)
5. American Society of Anesthesiologists grade 3, 4 or 5
6. Moderate to severe chronic kidney disease (preoperative eGFR < 60 mL/min/1.73 m2)
7. Massive hemorrhage to require blood transfusion during surgery
8. Severe hemodynamic instability to require continuous vasopressor infusion during surgery
9. Moderate to severe postoperative nausea and vomiting causing to stop additional narcotic analgesics within 24 h after surgery

Study & Design

• Study Type: Observational Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Total opioid consumption (morphine equivalent dose) during 24 h after surgery

Secondary Outcome Measures

Name	Time	Method
The evaluation of pain score (using Visual analogue scale) at 1 h, 6 h and 24 h after surgery;Complications during 24 h after surgery;Postoperative hospital stay (days)