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1.To determine the difference in VAS score between both the groups. 2.To determine the difference in time for need of first rescue analgesia and total number of doses of rescue analgesic required during first 72 hours postoperatively between both the groups.

Comparison of postoperative analgesia of intravenous tramadol vs transdermal buprenorphine patch in aortofemoral graft surgery - A randomized interventional study at SMS Medical College, Jaipur during 2020-21

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036226
Enrollment
60
Registered
2021-09-03
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: O- Medical and Surgical

Interventions

Intervention1: Transdermal Buprenorphine patch of 10 mg: Transdermal Buprenorphine patch of 10 mg with a delivery rate of 10 ug/hour Control Intervention1: Intravenous Tramadol 100 mg: Intravenous Tra

Sponsors

Sawai Man Singh Medical College And Attached Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients undergoing aorto-femoral graft surgery 2.Patient willing to give written informed consent 3.Patient of either sex 4.Weighing 40 to 70 kg â??BMI <40kg/m2

Exclusion criteria

Exclusion criteria: 1.Patient refusal 2.known or admitted alcohol or drug abusers 3.Allergic to drugs involved in study 4.Patient taking any drug that have interaction with tramadol and Buprenorphine

Design outcomes

Primary

MeasureTime frame
1.To determine the difference in VAS score between both the groups. 2.To determine the difference in time for need of first rescue analgesia and total number of doses of rescue analgesic required during first 72 hours postoperatively between both the groups. Timepoint: 72 hours—

Secondary

MeasureTime frame
1.To determine the difference in sedation score in both the groups 2.To assess and compare Hemodynamic parameters: (Heart Rate; Mean Blood Pressure; Systolic Blood Pressure; Diastolic Blood Pressure),. 3.To determine the difference in percentage of cases who develop side effects ( if any)in both groups in first 72 hours Timepoint: 72 hours—

Countries

India

Contacts

Public ContactASHISH KUMAR SHARMA

SMS Medical College Jaipur

reemadrrn@gmail.com9414398827

Outcome results

None listed

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