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Bupivacaine effect on analgesia subsequent to brachial plexus block

Phase 2
Conditions
Shoulder injuries.
Injuries to the shoulder and upper arm
S40-S49
Registration Number
IRCT2017050733848N1
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

patients aged between 20 to 65 years old candidate for shoulder surgery; Class I or II according to ASA classification. Exclusion criteria: consumption of anti-psychotic drugs; drug abusers; history of psychotic disorders; obstructive pulmonary diseases; body mass index greater than 30 kg/m2; emergent operations; change in anesthesia or surgery procedure due to severe complications.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patients pain severity after shoulder surgery during recovery. Timepoint: Postoperative recovery. Method of measurement: quadruple pain severity scale.;Patients pain severity after shoulder surgery during recovery. Timepoint: 6 hours, 12 hours and 24 hours after surgery. Method of measurement: Using visual analogue scale.;Duration of analgesia after shoulder surgery. Timepoint: Postoperative period. Method of measurement: Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Postoperative compliations hypotension. Timepoint: postoperative admission period. Method of measurement: Questionnaire.;Postoperative nausea and vomiting. Timepoint: during admission. Method of measurement: Questionnaire.
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