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A clinical interventional trial comparing a Regional block-External oblique intercostal Plane block against port site local infiltration in evaluating the postoperative pain management.The participants include laparoscopic right donor nephrectomy patients.

Phase 4
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2024/05/068030
Lead Sponsor
ParkaviV
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Age above 18 and below 70

Physical status classification:ASA1and ASA2

Both male and female

Patients who are willing to participate

Exclusion Criteria

Patients refusal

Allergic to local anaesthetic

History of multiple previous abdominal surgery

Study & Design

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