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Regional Anaesthesia for Inguinal Hernia Repair

Not Applicable
Completed
Conditions
Health Condition 1: null- ASA grade I / IIHealth Condition 2: K639- Disease of intestine, unspecified
Registration Number
CTRI/2015/08/006104
Lead Sponsor
ady Hardinge Medical Collee
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Healthy patients ASA grade I & II

Male

Unilateral inguinal Hernia ( Indirect or direct with fully reducible)

Exclusion Criteria

Patients having known cardivascular, respiartory, renal, hepatic or metabolic disease, active gastriintestinal reflux, mental dysfunction, morbid obesity, history of substance abuse, chronic analgesic use and history of analgesic use and history of allergy to local anaesthetics and infections at the block site

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The duration of post-operative analgesia was higher in paravertebral (PVB) group as compared to the spinal anaesthesia (SA). Also shorter time taken to reach the discharge criteria for home readiness in PVB group as compared to SA group.Timepoint: Both assessed postoperatively at 2, 4, 6, 12 and 24 hrs
Secondary Outcome Measures
NameTimeMethod
The incidence of side effects such as PONV, headache and urinary cathertisation were higher in SA group as to PVB. Significant decrease in blood pressure seen in SA as compared to the PVB block . No significant changes seen in heart rate and oxygen saturation.Timepoint: Incidence of side effect observe post operatively for 24 hrs. <br/ ><br>Hemodyanmic parameter - Baselie value, Immediately before block, Immediately after block, and then every three minutes for 1st 15 min and thereafter, at 10 min till the end of surgery
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