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Effectiveness of rectus sheath block in abdominal surgery

Not Applicable
Completed
Conditions
abdominal pain.
Abdominal and pelvic pain
Registration Number
IRCT2015052615696N2
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

inclusion :
age ;ASA class ; persian speaking and aggriation to htis study
exclusion :
disagriation ; infection or scar in insicion site ;sensitivity to bupivacaien ; chronic adiction ; any surgical pittwal or complications that not adequate for block ;sleep disorders ;sever obesity BMI over 33

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Poat operative pain. Timepoint: each 1 hour for 6 hour. Method of measurement: VAS.
Secondary Outcome Measures
NameTimeMethod
Post operative vomitting. Timepoint: each 1 h for 6 h. Method of measurement: number of ondansetron injection.;Post operative opiume use. Timepoint: each 1 h for 6 h. Method of measurement: loss of PCA as cc.
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