Health Condition 1: Z768- Persons encountering health services in other specified circumstances
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.patients between the age group of 1year and 8year of both sexes undergoing various infraumbilical surgeries 2. Patients belonging to ASA 1 and 2 grades 3.parental consent
Exclusion criteria
Exclusion criteria: 1.patients with known allergy to the study drugs 2. Suspected coagulopathy 3. Infection at site of caudal block 4.History of developmental delay and neurological diseases 5. Skeletal deformities in the caudal region 6.parental refusal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome of study will be assesment of Duration of analgesia (from the time of caudal injection to the time at which FLACC pain Pain score 4 or more)Timepoint: Duration of study will be around 1year | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome of study will be assesment of 1.postoperative sedation 2. Hemodynamic changes 3.total number of doses of rescue analgesia in 24 hoursTimepoint: Duration of study will be around 1year | — |
Countries
India
Contacts
Jawaharlal nehru medical college ,ajmer