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Comparing two pain relieving techniques (old technique and newer technique ) in patients undergoing surgery for disease in the major blood vessel of abdomen and groin

Comparison of epidural analgesia with ultrasound guided bilateral erector spinae plane block in aorto-femoral arterial bypass surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/017922
Enrollment
40
Registered
2019-03-06
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: I714- Abdominal aortic aneurysm, withoutrupture Health Condition 2: I723- Aneurysm of iliac artery Health Condition 3: I700- Atherosclerosis of aorta Health Condition 4: I740- Embolism and thrombosis of abdominal aorta Health Condition 5: I745- Embolism and thrombosis of iliac artery

Interventions

Intervention1: Epidural Analgesia: Epidural Analgesia in patients undergoing Aorto-femoral arterial bypass surgery Control Intervention1: Ultrasound guided Bilateral Erector spinae plane block: Ultras

Sponsors

Sri Jayadeva institute of Cardiovascular sciences and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing Aorto-femoral arterial bypass surgery

Exclusion criteria

Exclusion criteria: 1. Patient refusal. 2. Allergy to local anesthetics. 3. Localized infection. 4. Coagulopathy / Bleeding diathesis/ Patients on anticoagulants 5. Pre-existing neurological deficit 6. Spinal deformities 7. LV EF less than 40% 8. Cognitive impairment or an active psychiatric condition. 9. Inability to understand pain scoring. 10. Emergency surgery

Design outcomes

Primary

MeasureTime frame
To compare analgesic efficacy of epidural analgesia with ultrasound guided bilateral erector spinae plane block in patients undergoing aorto-femoral arterial bypass surgeryTimepoint: 48 hours post extubation—

Secondary

MeasureTime frame
to compare: improvement in pulmonary function and oxygenation. hemodynamic stability in peri operative period. adverse effects(PONV , pruritus, neurological deficits)Timepoint: 48 hours post extubation—

Countries

India

Contacts

Public ContactDr Ragavendran S

Sri Jayadeva institute of Cardiovascular sciences and research

dr.sragavendran@gmail.com919843994899

Outcome results

None listed

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