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A study to assess impact of modified ERAS and Conventional care in Small Bowel Perforations-RCT Study

A RANDOMIZED CONTROL TRIAL TO ASSESS IMPACT OF ADAPTED ERAS vs CONVENTIONAL CARE IN SMALL BOWEL PERFORATIONS. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070742
Enrollment
62
Registered
2024-07-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: K638- Other specified diseases of intestine Health Condition 2: K631- Perforation of intestine (nontraumatic)

Interventions

Intervention1: Primary objective- To compare Length of hospital (LOH) stay between the two groups (ERAS vs. Conventional care). Secondary objectives- Functional recovery parameters Time of removal of

Sponsors

DR PRABHAT RANJAN
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient of either gender with Age 18 to 60 years Patients having small bowel perforations Early presenting within 48 hours American Society of Anaesthesiologists (ASA) class I, II and III

Exclusion criteria

Exclusion criteria: Exclusion criteria 1Patients having perforations other than small bowel perforations 2.Not willing for giving consent 3.Operative indication of any other specialty Indications for restricted mobility and prolong per urethral catheter 3.Patient undergoing on mechanical ventilator for period greater than 24 hours 4.Organ failure in peri-op periods 5.Patients those required inotropes support for more than 24 hours 6.Pregnant female 7.Patient in septic shock at time of admission

Design outcomes

Primary

MeasureTime frame
To compare Length of hospital Stay (LOH)Timepoint: over the period of 30 days

Secondary

MeasureTime frame
Functional recovery parameters Time of removal of urinary catheter Time of Naso-gastric tube removal Time to start of ambulation Time of return of bowel sound Time of starting orally Time of removal of drain(if placed) Adherence to the Adapted-ERAS Morbidity Parameters Surgical site infection Need for extra analgesia Post operative nausea & vomiting ( PONV) incidence Need of extra analgesia Respiratory infection Timepoint: over the period of 30 days

Countries

India

Contacts

Public ContactDr Cherring tandup

PGIMER CHANDIGARH

ctandup@gmail.com8196991007

Outcome results

None listed

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