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Enhanced recovery protocols in Open Aortic surgeries

A study to assess the efficacy of Enhanced Recovery After Surgery (ERAS) protocol in Open Abdominal Aortic Surgery - A Prospective, Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062646
Enrollment
40
Registered
2024-02-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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: I700- Atherosclerosis of aorta

Interventions

Intervention1: ERAS group (Duration of intervention Preoperative till discharge - no fixed time period): Preoperative optimization of all comorbidities, Preoperative Counselling, Prophylactic IV anti

Sponsors

Sri Jayadeva Institute of Cardiovascular sciences and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed with aortoiliac occlusive diseases or abdominal aortic aneurysms who are fit for surgery Patients above the age of 18 years. ASA grade between 1 to 3.

Exclusion criteria

Exclusion criteria: Patients who required postoperative ICU admission. Patients undergoing surgeries other than open abdominal aortic surgeries in the same sitting. Patients requiring emergency surgery Patients allergic to Bupivacaine

Design outcomes

Primary

MeasureTime frame
Mean duration of Stay in Hospital (days) Timepoint: Mean duration of Stay in Hospital (end point will be calculated on the day of discharge - which will be variable )

Secondary

MeasureTime frame
Mean time for conversion from IV analgesics to Oral analgesics (days) Timepoint: days;Mean time to first bowel movement (days) Timepoint: How many days post op for bowel movement;Mean time to return to liquid and regular diet (days) Timepoint: hours;Post-operative opioid consumption (in mg) Timepoint: Total opiod consumption in mg at 12,24,36,48, 72 hours;Post-operative pain (using VAS)Timepoint: Numeric pain scoring at 6,12,24,36,48,72 hours;Rate of 45 days readmission (in percentage) Timepoint: Admission within 45 days

Countries

India

Contacts

Public ContactPoornima P

Sri Jayadeva institute of cardiovascular sciences and research

purni.purni0609@gmail.com7349669650

Outcome results

None listed

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