MedPath

A clinical trial to examine whether administering a low dose spinal anesthesia along with general anesthesia will give better pain relief in patients undergoing laparoscopic hernia repair.

Phase 3
Registration Number
CTRI/2010/091/000249
Lead Sponsor
S.Rajeshwari
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

(i) Adult males,Age 20 ? 65 years
(ii) Unilateral or bilateral reducible inguinal herniae
(iii) Scheduled for Total Extra Peritoneal (TEP) repair under geneal anesthesia

Exclusion Criteria

(i) Uncontrolled systemic illness
(ii) Neurological illness (Parkinsonism, h/o CVA)
(iii) Any contraindications to spinal anaesthesia (local infection, coagulopathy, documented anatomical abnormality, allergy to local anaesthetic agents)
(iv) Patients undergoing Trans Abdominal Pre Peritonal(TAPP)repair
(v) Irreducible herniae
(vi) Patients with other surgical procedures performed concurrently
(vii) Patient refusal for the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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