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Early Oral Refeeding in Mild Acute Pancreatitis (EORVsUOR)

Primary Purpose

Pancreatitis

Status
Completed
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
early oral refeeding
Sponsored by
Hospital Regional de Alta Especialidad del Bajio
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatitis focused on measuring Mild acute pancreatitis, Oral refeeding, Non inferiority clinical trial

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients admitted to the surgery services with diagnosis of acute biliary pancreatitis
  • Whit mild episode criteria and symptom onset time less than 24 hours

Exclusion Criteria:

  • Patients with pancreatitis from another cause other than biliary
  • Pregnant
  • History of chronic pancreatitis
  • Under 18 or over 75 years
  • With moderately severe or severe acute biliary pancreatitis

Sites / Locations

  • Hospital Regional de Alta Especilidad del bajio

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Early oral refeeding

Usual oral refeeding

Arm Description

Once the patient had a score of 1-3 of the analogue numerical scale (ENA), he was interrogated about symptoms such as nausea or vomiting, if he did not have them, then receives diet indicated between 16 and 24 hours after admission.

usual oral refeeding (UOR) Once the attending physician decided according to his clinical judgment to restart the oral feeding

Outcomes

Primary Outcome Measures

abdominal pain recurrence
Presence of abdominal pain after to oral refeeding

Secondary Outcome Measures

systemic inflammatory response
presence of systematic inflammatory response syndrome data, fever, leukocytosis

Full Information

First Posted
November 7, 2019
Last Updated
November 15, 2019
Sponsor
Hospital Regional de Alta Especialidad del Bajio
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1. Study Identification

Unique Protocol Identification Number
NCT04168801
Brief Title
Early Oral Refeeding in Mild Acute Pancreatitis
Acronym
EORVsUOR
Official Title
Non-inferiority Comparative Clinical Trial Between Early Oral Refeeding Versus Usual Oral Refeeding in Mild Acute Pancreatitis Patients
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
September 1, 2018 (Actual)
Primary Completion Date
June 1, 2019 (Actual)
Study Completion Date
June 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Regional de Alta Especialidad del Bajio

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background The aim of the study is to compare the onset of oral feeding in the first 24 hours after hospital admission and determine if this influences the recurrence of pain or alters the blood levels of pancreatic enzymes, compared to usual oral refeeding in patients with mild acute pancreatitis Methods This Non-Inferiority Randomized controlled trial was carried out between September 2018 and June 2019, prior authorization from the ethics committee in health research. Patients with diagnosis of mild acute biliary pancreatitis, were divided into: Group A (early oral refeeding) and Group B (usual oral refeeding). Outcome measures were lipase pancreatic, systemic inflammatory response (concentrations of leukocytes) were used as marker for it, feasibility evaluated by abdominal pain recurrence, presence and recurrence of gastrointestinal symptoms and length of hospital stay. The aim of the present study is to compare the onset of oral feeding in the first 24 hours after hospital admission and determine if this influences the recurrence of pain or alters the blood levels of pancreatic enzymes, compared to usual oral refeeding in patients with mild acute pancreatitis.
Detailed Description
BACKGROUND Acute pancreatitis (AP) is an inflammatory pancreatic process, presents different severity degrees [1]. Over the last two decades, there has been a paradigm shift in the management, from surgical to "step up" approach using percutaneous or endoscopic catheter drainage followed by minimally invasive necrosectomy [2]. As no curative therapy is currently available for AP, early treatment consists of supportive care which includes adequate fluid resuscitation, pain management and enteral nutrition [3]. Pancreatic rest by Nil Per Oral (NPO) strategy was considered necessary in AP till abdominal pain get resolved and the levels of pancreatic and inflammatory markers decrease [4]. This trend has changed, now it is clear that the early oral refeeding for PA mild does not only provide adequate caloric intake, it may also improve clinical outcomes. It has been hypothesized that the combination of disturbed intestinal motility, microbial overgrowth and increased permeability of the gut can lead to bacterial translocation, thus causing infection of pancreatic necrosis [5,6]. The oral refeeding (OR) may reduce translocation by stimulating intestinal motility, reducing bacterial overgrowth and thereby maintaining mucosal gut integrity [7,8]. Also decrease infection complications, organ failure and mortality as compared with routine total parenteral nutrition [9,10]. In patients with (predicted) mild pancreatitis, numerous studies concluded that a normal oral diet can be resumed once the pain is decreasing [11-13], However, it remains unclear what the optimal time to do it is. There is still no consensus about the definition of "early" refeeding. The aim of the present study is to compare the onset of oral feeding in the first 24 hours after hospital admission and determine if this influences the recurrence of pain or alters the blood levels of pancreatic enzymes, compared to usual oral refeeding in patients with mild acute pancreatitis. METHODS Patients This Randomized controlled trial was carried out between September 2018 and June 2019, prior authorization from the ethics committee in health research. A total number of 124 patients were randomized in this study. The sample size was calculated according to the formula published by Bouemn et all 2015 [14], in which a percentage of success was estimated with the standard treatment of 90% compared to the experimental management of 85%, with a margin of no less than 10%, with an alpha for a tail of 0.05%, and a beta of 20 %, with a percentage of estimated losses of approximately 10%, a total of 62 patients per group was obtained. Definitions The diagnosis of AP was established when the patient presents two or more of the following three findings: typical abdominal pain, elevation of serum pancreatic enzymes (amylase and/or lipase) at more than three times the upper limit of the normal value, and imaging study (ultrasonography or computed tomography) suggestive of AP [15]. Severity Assessment Severity assessment of AP was done based on the revised Atlanta classification into mild, moderately severe and severe. Absence of organ failure or local or systemic complications was labelled as mild AP; of was defined using the modified Marshall scoring system [16]; and only the patients whose complete these severity criteria were randomized for the study. Protocol Once the diagnosis of acute biliary pancreatitis was confirmed and the course was mild, corresponding informed consent signed. Fluid therapy with crystalloid solution (Hartmann), initial bolus of 10 mL / kg and followed by infusion for 24 h of 1.5 mL / kg / h. Pain management with opioid weak tramadol 50mg every 6 hours and paracetamol 1 gram every 8 hours with continuous evaluation of the analogue numerical scale to determine the need for extra doses Type of Diet: In both groups, their initial diet was the same so that this did not influence the results to be measured. The soft diet consisted of one of 900 Kcal per day, with 86.7% carbohydrates (190 g), 13.3% protein (30 g) and 0% lipids (0 g); during 24 h. When the diet was adequately tolerated and there was no evidence of clinical complications or deterioration, normal diet was indicated, and the follow-up continues. Data Collection: Laboratorial data, such as leukocytes, amylase and lipase were collected after inclusion in the study and after 24 and 48 h of oral refeeding. Clinical data records include age, gender, time from onset of pain baseline, Marshall score at admission and after start the oral feeding, gastrointestinal symptoms, abdominal pain, days until solid food intake, pain relapse, complications, length of hospital stay and readmissions. Statistical analysis Date are presented as frequency and percentage, comparisons between groups were using the χ2 test for binary data or Fisher´s exact test. Continuous variables are presented as median and range interquartile range and were compared using the Mann-Whitney U-test or t student test if they meet normal criteria. p-Values of less than 0.05 were considered significant. Statistical analyses were performed with SPSS version 25.0.0. Analysis by intention to treat was used.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatitis
Keywords
Mild acute pancreatitis, Oral refeeding, Non inferiority clinical trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prior authorization from the ethics committee in health research. Patients with diagnosis of mild acute biliary pancreatitis, were divided into: Group A (early oral refeeding) and Group B (usual oral refeeding). Outcome measures were lipase pancreatic, systemic inflammatory response (concentrations of leukocytes) were used as marker for it, feasibility evaluated by abdominal pain recurrence, presence and recurrence of gastrointestinal symptoms and length of hospital stay.
Masking
Outcomes Assessor
Masking Description
Only the person who performed the statistical analysis did not know to which group each patient belonged
Allocation
Randomized
Enrollment
124 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Early oral refeeding
Arm Type
Experimental
Arm Description
Once the patient had a score of 1-3 of the analogue numerical scale (ENA), he was interrogated about symptoms such as nausea or vomiting, if he did not have them, then receives diet indicated between 16 and 24 hours after admission.
Arm Title
Usual oral refeeding
Arm Type
Active Comparator
Arm Description
usual oral refeeding (UOR) Once the attending physician decided according to his clinical judgment to restart the oral feeding
Intervention Type
Dietary Supplement
Intervention Name(s)
early oral refeeding
Other Intervention Name(s)
Early Vs Usual oral refeeding
Intervention Description
Once the patient had a score of 1-3 of the analogue numerical scale (ENA), he was interrogated about symptoms such as nausea or vomiting, receives diet indicated between 16 and 24 hours after admission.
Primary Outcome Measure Information:
Title
abdominal pain recurrence
Description
Presence of abdominal pain after to oral refeeding
Time Frame
72 hours
Secondary Outcome Measure Information:
Title
systemic inflammatory response
Description
presence of systematic inflammatory response syndrome data, fever, leukocytosis
Time Frame
72 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients admitted to the surgery services with diagnosis of acute biliary pancreatitis Whit mild episode criteria and symptom onset time less than 24 hours Exclusion Criteria: Patients with pancreatitis from another cause other than biliary Pregnant History of chronic pancreatitis Under 18 or over 75 years With moderately severe or severe acute biliary pancreatitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edgard Lozada, Dr
Organizational Affiliation
Hospital Regional de Alta Especialidad
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Regional de Alta Especilidad del bajio
City
Leon
State/Province
Guanajuato
ZIP/Postal Code
37660
Country
Mexico

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
the database will be made available to corroborate results.
IPD Sharing Time Frame
1 year
IPD Sharing Access Criteria
will be sent via e-mail as soon as requested
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Early Oral Refeeding in Mild Acute Pancreatitis

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