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The effect of lidocaine on pain after abdominal hysterectomy surgery

Phase 2
Conditions
Single delivery by caesarean section.
O82.0
Registration Number
IRCT201207021306N6
Lead Sponsor
Vice chancellor for research-Guilan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
40
Inclusion Criteria

The exclusion criteria are: positive history of hepatits; cardiovascular diseases; hypersensitivity to local analgesic agents; history of conclusion; asthma; addiction; cancer and concomitant surgeries. Inclusion criterion: all patient who are candidate for abdominal of hysterectomy.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluation of Pain. Timepoint: At hours 8, 12, 24 and 48 hours after surgery and after surgery at the time of movement. Method of measurement: Visual pain scale.
Secondary Outcome Measures
NameTimeMethod
Side effects (dizziness, vomiting, nausea). Timepoint: Within 24 hours after surgery. Method of measurement: By Assistant.;Dosage of drugs. Timepoint: Within 24 hours after surgery. Method of measurement: By Assistant.;Satisfaction levels. Timepoint: Within 24 hours after surgery. Method of measurement: Ask the patient.
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