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Comparison of the effects of lidocaine and bupivacaine in preventing oculocardiac reflex in strabismus surgery

Phase 2
Conditions
Strabismus.
Unspecified strabismus
H50.9
Registration Number
IRCT20230122057174N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
120
Inclusion Criteria

ASA grade I or II (American Society of Anesthesiology classification)
Patients between 18 and 35 years old
Candidate patients for Sub-Tenon's block

Exclusion Criteria

Patients with ASA grade III or IV (American Society of Anesthesiology classification)
Positive history of heart disease
Positive history of hyperthyroidism
Positive history of coagulation disorders
Pregnant women
Patient refusal

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Heart rate. Timepoint: Every 5 minutes during the operation. Method of measurement: Monitoring.;Mean arterial pressure. Timepoint: Every 5 minutes during the operation. Method of measurement: Monitoring.;Pain. Timepoint: One hour after the operation. Method of measurement: Questionnaire and Numerical Pain Rating Scale (NRS).;Nausea. Timepoint: One hour after the operation. Method of measurement: History taking.;Vomiting. Timepoint: One hour after the operation. Method of measurement: History taking.
Secondary Outcome Measures
NameTimeMethod
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