Skip to content

The aim of this study was to comprare the minimum effective anesthetic concentration of mepivacaine in ultrasound-guided axillaryblock in patients with and without diabetic neuropathy.

Comparison of minimum effective anesthetic concentration of mepivacaine for axillary block in patients with and without diabetic neuropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0003017
Enrollment
44
Registered
2018-07-24
Start date
2018-08-01
Completion date
Unknown
Last updated
2020-03-23

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 : An axillary brachial plexus block is performed under ultrasound guidance. After sterilization of the armpit skin area of the upper part of the patient with chlorohexidine, an asept
lidocaine is used to partially anesthetize the needle. Place the 22G block needle in the in-plane method and center it in the brachial plexus. 1 ml of saline is injected first, and 30 ml of mepivacian

Sponsors

Inha University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: One group was a normal patient with no neurological abnormality in the upper extremities and the other group was a patient with diabetic neuropathy

Exclusion criteria

Exclusion criteria: Patients with contraindicated anesthesia (eg, coagulopathy, infection) Patients with a history of allergy to amide based local anesthetics If there is a neurological abnormality in the upper limb to undergo surgery If you are using a chronic (> 3 months) narcotic analgesic A pregnant patient By the definition of clinical trial committee of medical institutions where clinical trials are conducted, vulnerable subjects

Design outcomes

Primary

MeasureTime frame
block success

Secondary

MeasureTime frame
complication

Countries

Korea, Republic of

Contacts

Public ContactChunwoo Yang

Inha University Hospital

Outcome results

None listed

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