Comparison of analgesic efficacy between continuous adductor canal block and single adductor canal block followed by continuous intravenous fentanyl infusion in total knee arthroplasty

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CRIS

Registry ID

KCT0002121

Enrollment

Registered

2016-10-28

Start date

2016-08-22

Completion date

Unknown

Last updated

2019-03-11

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 : his was a randomized, double-blind, placebo-controlled study. Randomization into one of the two groups [Group ACB (continuous adductor canal block group) or Group SB (single shot w

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients between the ages of 20 and 90 years with an American Society of Anesthesiologists physical status 1-2 who were undergoing total knee arthroplasty with general anesthesia at our institution between july 2016 and july 2017 were assessed for study eligibility.

Exclusion criteria

Exclusion criteria: The exclusion criteria included a history of cardiovascular or respiratory disease, neurologic disorder, active alcohol or drug use, psychological disorder, obesity (body mass index = 35 kg/m2), ASA over 3, local anesthetic allergy, impaired renal function, impaired hematologic function and impaired hepatic function.

Design outcomes

Primary

Measure	Time frame
postoperative pain	—

Secondary

Measure	Time frame
motor weakness ;sensory deficit	—

Countries

Korea, Republic of

Contacts

Public ContactHwa Yong Shin

Chung-Ang University

paindoctor@daum.net+82-2-6299-2579

Outcome results