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To compare two methods of pain relief after the surgery in childre

Phase 1
Registration Number
CTRI/2018/08/015288
Lead Sponsor
Bangalore Baptist Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

•Age between 1 to 10 years

•weight of child less than 30kg

•American Society of Anesthesiologists (ASA) grade I and II patients

•Children posted for infraumbilical surgeries less than 2 hour duration (herniotomy, urethroplasty,circumcision, orchidopexy, lower limb orthopaedic surgeries etc)

Exclusion Criteria

1.Children posted for emergency surgery

2.Infection at the site of injection

3.Coagulopathy or on anticoagulation therapy

4.Congenital anomaly of lower spine and meninges

5.Active disease of the CNS

6.History of allergy to local anaesthetics, Clonidine and Dexamethasone

7.Surgeries in prone position

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the efficacy of ropivacaine with clonidine or dexamethasone as adjuvants for caudal epidural block in paediatric infraumbilical surgeries.Timepoint: To evaluate duration of analgesia (defined as time from caudal injection until the first requirement of rescue analgesia, pain assessed by FLACC). <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
1.To assess haemodynamic stability between the two groups. <br/ ><br>2.To assess incidence of any side effects like nausea and vomiting, sedation, bradycardia, hypotension, wound infection <br/ ><br>Timepoint: up to 12 hours postoperatively
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