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Optimizing the dose of intrathecal morphine in patients undergoing laparoscopic donor hepatectomy; a randomized non-inferiority trial

Optimizing the dose of intrathecal morphine in patients undergoing laparoscopic donor hepatectomy; a randomized non-inferiority trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0006526
Enrollment
56
Registered
2021-09-01
Start date
2021-08-29
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

None listed

Interventions

Drug : Drug name : Morphine Dose : 300mcg or 400mcg single shot before the surgery Intrathecal injection difference between group : morphine dose

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who undergo living donor hepatectomy for liver transplantation ASA physical status I or II

Exclusion criteria

Exclusion criteria: ASA physical status III or more Severe impaired coagulation profile (equal or more than INR 1.5 last coagulation test before the surgery) Patients who have unstable coronary disease or Congestive heart failure or Arrhythmia or cardiomyopathy Patients who have cerebrovascular disease Patients who have systemic infection or local infection on lumbar Chronic pain patients Patients who don't understand about study or refuse the study Patients who have history of severe psychological disease

Design outcomes

Primary

MeasureTime frame
Pain score (representing by 11-points Numerous Rating Scale)

Secondary

MeasureTime frame
Pain score (representing by 11-points Numerous Rating Scale);Opioid consumption;Nausea, Vomiting, Pruritus;Pain relief satisfaction;Sleep satisfaction;First gas-out time;Hypoventilation, Hypotension, Headache;The questionaire of QoR-15 score before and after the surgery

Countries

Korea, Republic of

Contacts

Public ContactJoan Seungwon Lee

Samsung Medical Center

seungwon0209.lee@samsung.com+82-2-3410-0369

Outcome results

None listed

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