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A COMPARATIVE STUDY OF  CAUDAL ANALGESIA WITH LEVOBUPIVACAINE 0.25 PERCENTAGE ALONE AND IN COMBINATION WITH 1 MICROGRAM FENTANYL OR CLONIDINE AMONG PAEDIATRIC PATIENTS

A COMPARATIVE STUDY OF  CAUDAL ANALGESIA WITH LEVOBUPIVACAINE 0.25PERCENTAGE ALONE AND IN COMBINATION WITH 1 MICROGRAM FENTANYL OR CLONIDINE AMONG PAEDIATRIC PATIENTS - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069190
Enrollment
105
Registered
2024-06-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Control Intervention1: NIL: NIL

Sponsors

Sapthagiri Institute of Medical Sciences and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1 and II Posted for sub umbilical surgical procedures receiving caudal block

Exclusion criteria

Exclusion criteria: Patients not willing to participate in the study. Patients with known allergy to study drugs. Suspected coagulopathy or bleeding diathesis ,local sepsis at the site of puncture. History of development delay.

Design outcomes

Primary

MeasureTime frame
To compare the duration of postoperative analgesia in levobupivacaine group with 1mcg dose fentanyl and clonidine groupsTimepoint: Measure HR,SPO2, BP every 5 minutes intraoperative and every 30 minutes postoperatively—

Secondary

MeasureTime frame
To estimate the cumulative analgesic requirement over 24 hrs in all the groups.Timepoint: Every 30 minutes first 2 hrs then 1 hourly for 24 hours—

Countries

India

Contacts

Public ContactPrabha P

Sapthagiri Institute of Medical Sciences and Research Centre

prabhap1510@gmail.com9448055973

Outcome results

None listed

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