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Retrolaminar block in unilateral inguinal hernioraphy

Phase 2
Recruiting
Conditions
Post operative pain control in unilateral inguinal hernia repair.
Inguinal hernia
Registration Number
IRCT20220212054002N2
Lead Sponsor
Mansoura university hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
50
Inclusion Criteria

Age between 20 and 60 years and prepared for elective unilateral inguinal hernioraphy.
American Society of anesthesiologists (ASA) I or II.

Exclusion Criteria

Patients refusal ASA > II.
Patients refusal h aving contraindications for the study medications.
Infections at block site.
History of substance abuse.
Mental dysfunction.
Metabolic disease
Using anticoagulants.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
umber of patients who needed rescue analgesia (morphine) in post operative. Timepoint: 24 hour post operative period. Method of measurement: Visual Analogue Scale to measure pain.
Secondary Outcome Measures
NameTimeMethod
Mean blood pressure ,and Heart rate. Timepoint: Basal(0), At skin incision, During sac traction, and At end of surgery. Method of measurement: Sphygmomonometer.;Post-operative pain. Timepoint: Immediate post-operative (0) and At 2, 4,6,8,12,24 h post-operative. Method of measurement: Visual Analogue Scale.
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