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A study to compare ropivacaine with fentanyl and bupivacaine fentanyl for caudal epidural in paediatric surgeries

Comparison of ropivacaine with fentanyl and bupivacaine with fentanyl for caudal epidural in paediatric infra umbilical surgeries - A prospective randomised study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023184
Enrollment
60
Registered
2020-02-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system

Interventions

Intervention1: Ropivacaine with Fentanyl: 0.25% of 0.7 ml/Kg Bupivacaine + 1mcg/Kg of Fentanyl with Normal Saline in Caudal Epidural Intervention2: Bupivacaine with Fentanyl: 0.25% of 0.7 ml/Kg Ropiva

Sponsors

Divya S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing infra umbilical surgeries of either sex American Society of Anaesthesiologist I or II

Exclusion criteria

Exclusion criteria: Patients allergic to local anesthetics/Fentanyl American Society of Anaesthesiologist III and above Patients with coagulation disorders Local site infection Congenital sacral anomalies Severe CVS abnormalities Renal or Hepatic Failure Neuromuscular disorder

Design outcomes

Primary

MeasureTime frame
To compare the time taken for regression of motor blockade in terms of post operative early ambulationTimepoint: Post Operative Period—

Secondary

MeasureTime frame
To assess intra operative and post operative hemodynamic stability upto 24 hours Duration of sensory analgesia and the time to the first demand for rescue analgesia Post Operative Nausea, Vomiting and Sedation ScoreTimepoint: Intra Operative Period and Post Operative Period—

Countries

India

Contacts

Public ContactDivya S

Shri Sathya Sai Medical College and Research Institute

esenkeyem@gmail.com9786743120

Outcome results

None listed

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