To determine the difference in MEAN TIME DURATION FOR THE NEED OF FIRST RESCUE ANALGESIA AMONG THE TWO GROUPS.

Not yet recruiting

• Conditions: Medical and Surgical. Ayurveda Condition: not applicable,

• Registration Number: CTRI/2021/02/030958
• Lead Sponsor: Sawai Man Singh Medical College And Attached Hospitals

Brief Summary

By studying and comparing effects of above mentioned doses of Dexmedetomidine and Tramadol as an adjuvant agents for Caudal block in Infra Umbilical surgeries will help us to

be more effcient in providing best anesthesia possible to the patient and open up to more research projects.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2021-01-30
• Study Start: 2021-05-02

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• 1.Children undergoing elective infraumblical surgery 2.Age ranging between 1-7 years of either sex.
• 3.ASA grade I&II.
• 4.Children weight between 7 to 25 kg.

Exclusion Criteria

• 1.History of allergic reactions to drugs used in study.
• 2.Patients on anticoagulant therapy and H/O coagulation disorders.
• 3.Local infection at the proposed site of puncture for caudal anaesthesia.
• 4.Lack of consent by parents/guardian 5.History of developmental delay.
• 6.History of neurological deficit or vertebral deformity.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To determine the difference in mean time duration for the need of first rescue analgesia among the two groups.	24 HOURS

Secondary Outcome Measures

Name	Time	Method
1.To assess and compare Hemodynamic changes: -HR, MBP, SBP and DBP.	2.Difference in mean CHEOPS Score at different time intervals.

Trial Locations

Locations (1)

SMS MEDICAL COLLEGE AND HOSPITAL.; 🇮🇳 Jaipur, RAJASTHAN, India

SMS MEDICAL COLLEGE AND HOSPITAL.

🇮🇳Jaipur, RAJASTHAN, India

Dr Bajrang yadav

Principal investigator

9602757227

bajrangyadav2@gmail.com