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ERAS vs Conventional Approach in Peptic Perforation-RCT

Enhanced Recovery After Surgery Versus Conventional Approach in Peptic Perforation-A Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04194060
Acronym
ERASE
Enrollment
60
Registered
2019-12-11
Start date
2020-01-20
Completion date
2021-06-15
Last updated
2022-03-18

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

Conditions

Emergencies, Peptic Ulcer Perforation, Perforated Bowel, Perioperative Complication, Post-Op Complication

Keywords

ERAS, Emergency surgery, Fast track surgery, Perioperative Care, Enhanced recovery after surgery

Brief summary

This study compares 2 different ways of perioperative management in patients of peptic perforation. Experimental arm is the ERAS arm( Enhanced recovery after surgery) and the comparative arm is Conventional arm.

Detailed description

While the conventional approach to perioperative management can potentially prolong the post operative hospital stay, ERAS(Enhanced recovery after surgery), a multi-modal and multispeciality approach to perioperative management may reduce the length of hospital stay. In the preoperative period, patients will be counselled regarding the operative procedure and particulars of the perioperative management.In the intra-operative period short acting general anesthetic agents and short acting muscle relaxants will be used.Intravenous fluid administration will be goal directed. After the operative procedure, bilateral rectus sheath block will be administered. Patient will also receive post-operative nausea and vomiting prophylaxis. Nasogastric tube will be removed immediately after the operative procedure. In the post operative period, patients will be encouraged to ambulate early. Enteral nutrition will be initiated as early as possible. Indwelling catheters will be removed in the early post-operative procedure.

Interventions

COMBINATION_PRODUCTEnhanced Recovery after Surgery group

* Tracheal intubation and with General anesthesia * Short acting anesthetic agents,avoid opioid agents * Omental patch repair with placement of sub hepatic drain * Bilateral Transverse abdominis plane block/ Rectus sheath block immediately after surgery. * Post operative nausea and vomiting prophylaxis. * Encourage to mobilize out of bed after effect of general anesthesia has weaned off. * Initiation of feeding-Oral sips on day 1, step up day 2 onward * Removal of nasogastric tube-immediately after surgery after aspirating the gastric content through nasogastric tube. * Removal of urinary catheter-after weaning from the effect of general anesthesia. * Sub hepatic drain removal -anytime within 24 hours;drain will not be removed if fluid is bilious or pus. * Avoid opiod analgesics.

COMBINATION_PRODUCTConventional

Tracheal intubation * Short acting anesthetic agents, avoid opiod anesthesia agents. * Omental patch repair along with sub hepatic drain placement. * Post operative nausea and vomiting prophylaxis. * Ambulation-as per patients' own request. * Initiation of oral feed- after passage of 1st flatus. * Nasogastric tube removal-output \<300ml/day with resolution of ileus. * Removal of urinary catheter- when patient sits on bed side/ambulate. * Removal of sub hepatic drain-when patient tolerates unrestricted amount of liquid diet and drain output is less than 200 ml /day. * Patient will receive opiod analgesics.

Sponsors

All India Institute of Medical Sciences, Bhubaneswar
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Patient will be allocated into two arms, ERAS(Enhanced recovery after surgery) group and Conventional group. 30 patients will be recruited in each arm.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Patient diagnosed with peptic perforation intra -operatively 2. Perforation of size \<=1 cm 3. Patient age more than 18 years 4. American Society of Anesthesiologists score of I or II

Exclusion criteria

1. Refractory septic shock at presentation. 2. Known Chronic kidney disease/ Chronic liver disease patients 3. Pregnant patients. 4. Patients with history of chronic steroid abuse. 5. Intraoperatively * Patient with coexistent peptic perforation with bleeding ulcer. * Peptic perforation requiring procedure other than Omental patch repair. * Sealed perforations. * Malignant perforation. 6. Patient requiring Positive Pressure Ventilator support post operatively for more than 12 hours. 7. Patient requiring urinary catheterization for other indications. 8. Coexistent neurological or psychiatric illness or unable to understand the study. 9. Patient refusing for consent.

Design outcomes

Primary

MeasureTime frameDescription
Length of hospital stayPost operative period up-to one month.Duration from the time of operation to time of discharge

Secondary

MeasureTime frameDescription
Recovery of functional parametersPost operative period up-to one month.* Time of withdrawal of nasogastric tube (hours) * Time to first bowel sound (hours) * Time to first flatus (hours) * Time to first stool (hours) * Time to removal of drain(hours) * Time to first fluid diet (hours) * Time to first solid diet (hours) * Time to stoppage of IV fluids(hours) * Time of removal of urinary catheter (hours) * Time to ambulation(hours)
Post operative complicationsPost operative period up-to three months.* Anastomotic leakage * Pneumonia * Ileus * Obstruction * Wound infection * Abdominal sepsis * Burst Abdomen * Need for reinsertion of nasogastric tube * Need for reinsertion of urinary catheter * Need for drainage of abdominal collection * Readmission * Re operation * Mortality

Other

MeasureTime frameDescription
Quality of life scoring and assessmentPost operative period - at day of discharge, at one month follow up and at third month follow up.Quality of life assessment will be done using EQ-5D-5L questionnaire (Euroqol 5 dimensions and 5 levels). It has 2 components, descriptive and objective. Descriptive component comprises of 5 dimensions which are mobility, self care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels, namely no problem, slight problems, moderate problems, severe problems and extreme problems. Objective component is also called Euroqol visual analog scale. Score ranges from zero to hundred.The endpoints are labelled as 'the best health participant can imagine' and 'the worst health participant can imagine'. It will be assessed on the day of discharge, follow up at one month and follow up at third month in the post operative period.
Intra-abdominal collectionPost operative period-at one month and at third month in post operative period.Ultrasonography abdomen will be done at one month to look for any intra-abdominal collection and if any collection is found, will be repeated at third month follow up.
Hematological parameterPost-operative period up-at one month and at third month.Total leukocyte count will be measured at follow up at one month.If the value is more than 11,000 cells/mm cube or less than 4000 cells/mm cube, then it will be measured again at third month of follow up.

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026