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A rondomized control trial to assess the impact of Modified Enhanced recovery after surgery(ERAS-new surgical protocol which reduces surgical stress and facilitate early recovery)protocol vs Non-ERAS protocol in Acute Intestinal obstruction

A Randomized control trail to assess the impact of Modified Enhanced recovery after surgery(ERAS) protocol vs Non-ERAS protocol in Acute Intestinal obstruction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/042156
Enrollment
60
Registered
2022-04-26
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K410- Bilateral femoral hernia, with obstruction, without gangrene Health Condition 2: K400- Bilateral inguinal hernia, with obstruction, without gangrene Health Condition 3: K563- Gallstone ileus Health Condition 4: K567- Ileus, unspecified Health Condition 5: K565- Intestinal adhesions [bands] withobstruction (postinfection) Health Condition 6: K561- Intussusception Health Condition 7: K566- Other and unspecified intestinal obstruction Health Condition 8: K564- Other impact

Interventions

Intervention1: ERAS: Enhanced recovery after surgery (ERAS) is a multidisciplinary, evidence-based, standardized approach to minimize the stress response to surgery, promote organ function and subsequ

Sponsors

Post Graduate Institute of Medical Education and Research Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patient coming to the emergency with acute intestinal obstruction will be included

Exclusion criteria

Exclusion criteria: Patient presenting with Refractory shock, bowel perforation, Organ Failure in Peri-operative Period, Pregnant Females. Post-operative Mechanical Ventilator Support > 24 hours.

Design outcomes

Primary

MeasureTime frame
Short Term Post-Operative Morbidity,30-day Mortality Rate, 30-day Readmission Rate, Length of hospital (LOH) stay Timepoint: 4 weeks

Secondary

MeasureTime frame
Time to Start Ambulation, Naso-gastric tube removal, Return of Bowel sound,Passage of First Flatus and stool,Tolerating Oral liquids and solids, Visual analog scale for pain, Removal of Urinary catheter and other Drains Timepoint: from day of surgery to day of discharge

Countries

India

Contacts

Public ContactDr Ankit Aggarwal

Post Graduate institute of medical education and research

sakaraypgi@gmail.com7087008268

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 8, 2026