Pudendal Nerve Block With Clonidine in Pediatric Perineal Surgeries

Analgesic Efficacy Of Ultrasound Guided Pudendal Nerve Block v/s Caudal Block In Pediatric Perineal Surgeries- A Prospective Randomized Comparative Study - NIL

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061937

Enrollment

Registered

2024-01-29

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N481- Balanitis Health Condition 2: O- Medical and Surgical Health Condition 3: N471- Phimosis

Interventions

Intervention1: Pudendal Nerve block: 0.2 ml/kg of 0.2% ropivacaine and 1 mcg/kg of clonidine For 24 hours post block Control Intervention1: Caudal Nerve Block: 1 ml/kg of 0.2% ropivacaine and 1 mcg/

Eligibility

Inclusion criteria

Inclusion criteria: Aged 6 months to 6 year (ASA) physical status I - II Scheduled to undergo elective perineal surgeries - circumcision, hypospadiasis, PUJ fulgration, chordee repair

Exclusion criteria

Exclusion criteria: Parent refusal History of allergic reactions to local anesthetics Bleeding diatheses Rash or Infection at the injection site Anatomical spinal abnormality Liver diseases

Design outcomes

Primary

Measure	Time frame
Duration of analgesia after block Number of rescue doses required in 24 hoursTimepoint: Base line, 30 mins, 1 hour, 1.5hour, 2 hour, 2.t hour, 3 hour, 6 hour, 9 hour, 12 hour, 18 hour, 24 hour	—

Secondary

Measure	Time frame
Parent satisfaction Timepoint: End of 24 hours	—

Countries

India

Contacts

Public ContactDr. Akilandeswari,

Sri Ramachandra Institute of Higher Education and Research

akilaanes@gmail.com9840636238

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026