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Analgesic efficacy of intrathecal morphine and bupivacaine during the early postoperative period in patients who underwent robotic-assisted laparoscopic prostatectomy

Spinal morphine and bupivacaine for postoperative analgesia following robot-assisted laparoscopic prostatectomy : a prospective randomized controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004350
Enrollment
50
Registered
2019-10-17
Start date
2019-10-09
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

None listed

Interventions

Drug : In the experimental group, general anesthesia was performed after a single administration of intrathecal morphine 7.5 mcg and bupivaaine 7.5mg. In the control group, general anesthesia was perf

Sponsors

The Catholic University of Korea, Seoul St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: 1. Disagreement to participate in this study 2. Emergency surgery 3. Children (under 19 years old) 4. Old (over the 75 years old) 5. American Society of Anesthesiologists grade 3, 4 or 5 6. Massive hemorrhage to require blood transfusion during surgery 7. Severe hemodynamic instability to require continuous vasopressor infusion during surgery 8. Moderate to severe postoperative nausea and vomiting causing to stop additional narcotic analgesics within 24 hours after surgery

Design outcomes

Primary

MeasureTime frame
total opioid consumption (morphine milligram equivalents) in the first 24 hours

Secondary

MeasureTime frame
The evaluation of pain at 1 hour, 6 hour, and 24 hour after surgery (Numeric Rating Scale);Complications occurs for 24 hours after surgery

Countries

Korea, Republic of

Contacts

Public ContactJung-Woo Shim

The Catholic University of Korea, Seoul St. Mary's Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 23, 2026