A randomized non-inferiority clinical trial comparing intrathecal morphine and erector spinae block for analgesia in living donors for liver transplantation

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0003191

Enrollment

Registered

2018-09-20

Start date

2018-07-09

Completion date

Unknown

Last updated

2019-04-23

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

Conditions

None listed

Interventions

Procedure/Surgery : Patients are randomly allocated to the 2 groups: the erector spinae plane block group and intrathecal morphine group.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Adult (=19 years old or >19 years old) American society of anesthesiologist physical status I, II: healthy (I), controlled systemic disease (II)

Exclusion criteria

Exclusion criteria: American society of anesthesiologist physical status higher than III: uncontrolled systemic disease (III), severe systemic disease (IV), death (V) Child (<18 years old or =18 years old) Old Age (=70 years old or> 70 years old) Pregnancy Coagulopathy Unstable coronary artery disease, congestive heart failure, arrythmia, cardiomyopathy Cerebrovascular disease Systemic infection, infection at site of erector spinae plane block chronic pain disorder Refusal to study Allergy to local anesthetics Psychiatric disease

Design outcomes

Primary

Measure	Time frame
pain score at 24 hour postoperatively	—

Secondary

Measure	Time frame
Opioid consumption during the 24 h postoperatively	—

Countries

Korea, Republic of

Contacts

Public ContactRyungA Kang

Samsung Medical Center

ryunga.kang@gmail.com+82-2-3410-2470

Outcome results