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A study to compare the pain relief by two modalities pudendal and caudal block in children undergoing genital surgeries.

Phase 4
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/11/060126
Lead Sponsor
Post Graduate Institute of Medical Education and Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Age 2-7 years

2.ASA 1 and 2 patients

3.Undergoing penile surgeries( urethroplasty, chordee correction, and correction of urethrocutaneous fistula) under general anesthesia

Exclusion Criteria

1.Presence of a congenital heart disease

2.Presence of respiratory, renal, or hepatic dysfunction

3.ASA III and IV

4.Local infection

5.Coagulopathy

Study & Design

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