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Ketamine and post operative pai

Phase 3
Conditions
regional anesthesia.
Local anaesthetics
Registration Number
IRCT2013091414661N1
Lead Sponsor
Isfahan University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Inclusion criteria : Patients with age between 15 and 60 years ; American Society of Anesthesiologists (ASA) classes I - II ; and body mass index (BMI) between 20 and 35 kg/m2.
Exclusion criteria : preexisting neuropathy, coagulopathy ; hepatic or renal impairment ; severe pulmonary disease ; allergy to drugs used in this study ; infection at the injection site ; pregnancy or lactation ; prior surgery in the supraclavicular, infraclavicular or axillary regions ; alcohol or drug abuse ; duration of operation more than 120 min or less than 30 min ; refusal of the patient.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Post operative pain. Timepoint: the first 24hours post operatively. Method of measurement: VAS.
Secondary Outcome Measures
NameTimeMethod
Onset times and duration of sensory and motor block. Timepoint: intra operative. Method of measurement: by chornometer.
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