Simvastatin in the Prevention of Recurrent Pancreatitis (SIMBA-16)
Primary Purpose
Pancreatitis Relapsing
Status
Unknown status
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Simvastatin 40mg
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Pancreatitis Relapsing focused on measuring Pancreatitis, Acute pancreatitis, Chronic pancreatitis, Simvastatin, Recurrent
Eligibility Criteria
Inclusion Criteria:
- Adult (>=18) patients
- At least 2 episodes of acute pancreatitis or acute flares of chronic pancreatitis
- Written consent to participate in the study
Exclusion Criteria:
- <2 episodes of pancreatitis in the last 12 months.
- Statin consumption in the previous year.
- Contraindications to the use of Statins
- Cholelithiasis or choledocholitiasis diagnosed in the last episode of pancreatitis
- Endoscopic sphyncterotomy and/or cholecystectomy and/or pancreatic surgery between last episode of AP and recruitment or patients who are expected to undergo one of this techniques in less than a year.
- Serum triglycerides >500 mg/dL without previous specific treatment before the last episode of pancreatitis, or in patients expected to have a change in their specific hypertriglyceridemia treatment in less than 1 year
- Primary hyperparathyroidism that has been operated between last episode of pancreatitis and recruitment or will be operated in less than 1 year
- Iatrogenic Pancreatitis
- Abstinence syndrome due to alcohol or drugs and/or delirium tremens in the last 6 months before recruitment
- Previous (last year) failure to attend follow-up medical visits, social problems that may be associated to failure to take the medication or to perform an adequate follow-up
- Pregnancy, breastfeeding
Sites / Locations
- AlicanteRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo
Simvastatin
Arm Description
placebo 1 year
40 mg 1 year
Outcomes
Primary Outcome Measures
Primary end point
Recurrence of pancreatitis during the follow-up period. Pancreatitis is defined as 2 or more of the following criteria: I) increased amylase and/or lipase in blood higher than 3 times the upper limit of normality, II) typical abdominal pain and III) signs of acute pancreatitis or acute flare of inflammation in chronic pancreatitis on imaging (CT scan or MRI).
Secondary Outcome Measures
Secondary end point
New-onset diabetes at the end of follow-up, according to the American Diabetes Association criteria. Blood levels of glycosylated hemoglobin at the end of follow-up will also be compared to baseline (beginning of the study)
New-onset exocrine pancreatic insufficiency
New-onset exocrine pancreatic insufficiency defined by fecal elastase-1 <100 mcg/g. Fecal elastase-1 levels at the end of follow-up will also be compared to baseline
Chronic Pancreatitis on imaging
Chronic Pancreatitis on imaging at the end of follow-up, defined as calcifications and/or dilated pancreatic duct (≥4mm) on a CT scan
All-cause hospital admissions
Frequency of all-cause hospital admissions
Severity of pancreatitis
Severity of pancreatitis according to the revision of the Atlanta Classification (moderate-to-severe versus mild)
Adherence to treatment
Percentage of the planned treatment consumed by the patient
Adverse events
Frequency of adverse events
Full Information
NCT ID
NCT04021498
First Posted
July 12, 2019
Last Updated
September 22, 2019
Sponsor
Enrique de-Madaria
Collaborators
Instituto de Salud Carlos III, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana, Generalitat Valenciana
1. Study Identification
Unique Protocol Identification Number
NCT04021498
Brief Title
Simvastatin in the Prevention of Recurrent Pancreatitis
Acronym
SIMBA-16
Official Title
Simvastatin in the Prevention of Recurrent Pancreatitis, a Triple Blind, Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Unknown status
Study Start Date
September 29, 2017 (Actual)
Primary Completion Date
July 29, 2022 (Anticipated)
Study Completion Date
September 28, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Enrique de-Madaria
Collaborators
Instituto de Salud Carlos III, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana, Generalitat Valenciana
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
Recurrent acute pancreatitis and recurrent relapses of inflammation in chronic pancreatitis are an important problem. In some cases, prevention of these acute flares of inflammation is not possible. Population-based studies and meta-analysis of randomized controlled trials suggest that statins may decrease the incidence of acute pancreatitis. SIMBA aims to investigate the effect of simvastatin on the incidence of new episodes of pancreatitis in recurrent acute pancreatitis and chronic pancreatitis. This is a non-profit, researcher-driven placebo-controlled multicenter (27 Spanish centers) randomized controlled trial
Detailed Description
Acute pancreatitis (AP) is the 3rd cause of hospital admission due to gastrointestinal disease. Approximately 20% of the patients will relapse after a first episode of AP. The low frequency of relapse in biliary AP is due to the high effectiveness of cholecystectomy but a first episode of AP due to alcoholic or other etiologies is associated with relapse in one every four patients. Currently, besides counselling for alcohol and tobacco abstinence, there is no specific medical treatment that changes the natural history of recurrent AP. Recurrent AP is an intermediary stage in the pathogenesis of chronic pancreatitis (CP) and a subset of recurrent AP patients during their natural course transition to CP (one every three patients). Forty-five percent of patients with CP experience intermittent flares of pain. Simvastatin has been associated to a decrease in the incidence of AP in a population-based study (Wu et al, Gut. 2015) and in a meta-analysis of randomized controlled trials (Preiss et al, JAMA 2012).
The main aim of SIMBA (SIMvastatin in the prevention of recurrent pancreatitis, a triple Blind rAndomized controlled multicenter trial) is to compare the recurrence rate of pancreatitis in patients with established recurrent pancreatitis (acute pancreatitis and acute flares in chronic pancreatitis) consuming simvastatin versus placebo.
The secondary aims are 1) to compare in patients with recurrent AP at the end of follow-up period the progression to chronic pancreatitis on imaging (calcifications and/or dilated ductal system), as well as endocrine and exocrine pancreatic function; 2) to compare the severity of recurrent pancreatitis between both treatment arms.
Design: SIMBA is a triple-blind randomized placebo-controlled, parallel-group, superiority multicenter (27 Spanish centers) trial. This final protocol (version 4) was finished on June 20th 2018.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatitis Relapsing
Keywords
Pancreatitis, Acute pancreatitis, Chronic pancreatitis, Simvastatin, Recurrent
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
144 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo
1 year
Arm Title
Simvastatin
Arm Type
Experimental
Arm Description
40 mg
1 year
Intervention Type
Drug
Intervention Name(s)
Simvastatin 40mg
Other Intervention Name(s)
Brand name: Simvastatin Normon, 40 mg
Intervention Description
phase III, triple-blind randomised placebo-controlled trial comparing simvastatin 40 mg/day versus placebo (lactose). One hundred and fifty eight patients with recurrent AP (at least 2 episodes) will be included (79 per arm of treatment). Treatment and follow-up will last for 12 months.
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
lactose (brand name: lactosa monohidrato Fagrón)
Intervention Description
phase III, triple-blind randomised placebo-controlled trial comparing simvastatin 40 mg/day versus placebo (lactose). One hundred and fifty eight patients with recurrent AP (at least 2 episodes) will be included (79 per arm of treatment). Treatment and follow-up will last for 12 months.
Primary Outcome Measure Information:
Title
Primary end point
Description
Recurrence of pancreatitis during the follow-up period. Pancreatitis is defined as 2 or more of the following criteria: I) increased amylase and/or lipase in blood higher than 3 times the upper limit of normality, II) typical abdominal pain and III) signs of acute pancreatitis or acute flare of inflammation in chronic pancreatitis on imaging (CT scan or MRI).
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Secondary end point
Description
New-onset diabetes at the end of follow-up, according to the American Diabetes Association criteria. Blood levels of glycosylated hemoglobin at the end of follow-up will also be compared to baseline (beginning of the study)
Time Frame
1 year
Title
New-onset exocrine pancreatic insufficiency
Description
New-onset exocrine pancreatic insufficiency defined by fecal elastase-1 <100 mcg/g. Fecal elastase-1 levels at the end of follow-up will also be compared to baseline
Time Frame
1 year
Title
Chronic Pancreatitis on imaging
Description
Chronic Pancreatitis on imaging at the end of follow-up, defined as calcifications and/or dilated pancreatic duct (≥4mm) on a CT scan
Time Frame
1 year
Title
All-cause hospital admissions
Description
Frequency of all-cause hospital admissions
Time Frame
1 year
Title
Severity of pancreatitis
Description
Severity of pancreatitis according to the revision of the Atlanta Classification (moderate-to-severe versus mild)
Time Frame
1 year
Title
Adherence to treatment
Description
Percentage of the planned treatment consumed by the patient
Time Frame
1 year
Title
Adverse events
Description
Frequency of adverse events
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult (>=18) patients
At least 2 episodes of acute pancreatitis or acute flares of chronic pancreatitis
Written consent to participate in the study
Exclusion Criteria:
<2 episodes of pancreatitis in the last 12 months.
Statin consumption in the previous year.
Contraindications to the use of Statins
Cholelithiasis or choledocholitiasis diagnosed in the last episode of pancreatitis
Endoscopic sphyncterotomy and/or cholecystectomy and/or pancreatic surgery between last episode of AP and recruitment or patients who are expected to undergo one of this techniques in less than a year.
Serum triglycerides >500 mg/dL without previous specific treatment before the last episode of pancreatitis, or in patients expected to have a change in their specific hypertriglyceridemia treatment in less than 1 year
Primary hyperparathyroidism that has been operated between last episode of pancreatitis and recruitment or will be operated in less than 1 year
Iatrogenic Pancreatitis
Abstinence syndrome due to alcohol or drugs and/or delirium tremens in the last 6 months before recruitment
Previous (last year) failure to attend follow-up medical visits, social problems that may be associated to failure to take the medication or to perform an adequate follow-up
Pregnancy, breastfeeding
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alicia Vaillo
Phone
0034 965933468
Email
vailloalicia@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Enrique de-Madaria, MD PhD
Organizational Affiliation
Gastroenterology Department, Hospital General Universitario de Alicante, Spain
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alicante
City
Alicante
ZIP/Postal Code
03010
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alicia Vaillo
Phone
0034 965933468
Email
vailloalicia@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33644082
Citation
Cardenas-Jaen K, Vaillo-Rocamora A, Gracia A, Garg PK, Zapater P, Papachristou GI, Singh VK, Wu BU, de-Madaria E. Simvastatin in the Prevention of Recurrent Pancreatitis: Design and Rationale of a Multicenter Triple-Blind Randomized Controlled Trial, the SIMBA Trial. Front Med (Lausanne). 2021 Feb 10;7:494. doi: 10.3389/fmed.2020.00494. eCollection 2020.
Results Reference
derived
Learn more about this trial
Simvastatin in the Prevention of Recurrent Pancreatitis
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