Emergencies Clinical Trial
— ERASEOfficial title:
Enhanced Recovery After Surgery Versus Conventional Approach in Peptic Perforation-A Randomized Control Trial
Verified date | March 2022 |
Source | All India Institute of Medical Sciences, Bhubaneswar |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 60 |
Est. completion date | June 15, 2021 |
Est. primary completion date | May 15, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
India | Tushar S Mishra | Bhubaneswar | Odisha |
Lead Sponsor | Collaborator |
---|---|
All India Institute of Medical Sciences, Bhubaneswar |
India,
Agarwal A, Jain S, Meena LN, Jain SA, Agarwal L. Validation of Boey's score in predicting morbidity and mortality in peptic perforation peritonitis in Northwestern India. Trop Gastroenterol. 2015 Oct-Dec;36(4):256-60. — View Citation
Gonenc M, Dural AC, Celik F, Akarsu C, Kocatas A, Kalayci MU, Dogan Y, Alis H. Enhanced postoperative recovery pathways in emergency surgery: a randomised controlled clinical trial. Am J Surg. 2014 Jun;207(6):807-14. doi: 10.1016/j.amjsurg.2013.07.025. Ep — View Citation
Lohsiriwat V, Jitmungngan R. Enhanced recovery after surgery in emergency colorectal surgery: Review of literature and current practices. World J Gastrointest Surg. 2019 Feb 27;11(2):41-52. doi: 10.4240/wjgs.v11.i2.41. — View Citation
Mohsina S, Shanmugam D, Sureshkumar S, Kundra P, Mahalakshmy T, Kate V. Adapted ERAS Pathway vs. Standard Care in Patients with Perforated Duodenal Ulcer-a Randomized Controlled Trial. J Gastrointest Surg. 2018 Jan;22(1):107-116. doi: 10.1007/s11605-017-3474-2. Epub 2017 Jun 26. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Quality of life scoring and assessment | 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. | Post operative period - at day of discharge, at one month follow up and at third month follow up. | |
Other | Intra-abdominal collection | 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. | Post operative period-at one month and at third month in post operative period. | |
Other | Hematological parameter | 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. | Post-operative period up-at one month and at third month. | |
Primary | Length of hospital stay | Duration from the time of operation to time of discharge | Post operative period up-to one month. | |
Secondary | Recovery of functional parameters | 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 period up-to one month. | |
Secondary | Post operative complications | 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 |
Post operative period up-to three months. |
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