- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03667703
Stress Ulcer Prophylaxis Versus Placebo in Critically Ill Infants With Congenital Heart Disease (SUPPRESS-CHD)
Stress Ulcer Prophylaxis Versus Placebo - a Blinded Randomized Control Trial to Evaluate the Safety of Two Strategies in Critically Ill Infants With Congenital Heart Disease
Study Overview
Status
Intervention / Treatment
Detailed Description
Background & Significance. Approximately 36,000 infants are born with congenital heart disease (CHD) in the United States each year, often requiring surgical intervention in the first year of life. They are vulnerable to postoperative morbidities including infection, growth failure and neurodevelopmental delay. Upon admission to the cardiac intensive care unit (CICU), infants are routinely prescribed stress ulcer prophylaxis (SUP) to decrease acid release from the stomach thus preventing ulcer-induced upper gastrointestinal (UGI) bleeding. Although adopted from the adult literature, this practice is expensive and has not been shown to be effective in infants. More importantly, recent literature suggests that this may not be safe. Studies show an increased risk of hospital-acquired infections, necrotizing enterocolitis and alterations in the evolving healthy gut flora in infants. The study investigators have recently demonstrated an increased risk of infection in children receiving SUP and also reported differences in microbial diversity among children in the CICU. It is necessary to proceed with a prospective trial to determine the safety of withholding SUP in critically ill children with CHD.
Specific Aims & Hypothesis. The overarching hypothesis of the proposal is withholding SUP from critically ill infants with CHD is safe and results in favorable microbial diversity, thus decreasing hospital-acquired infections. Primary Aim 1 of the study is to assess the feasibility of this pilot randomized, controlled clinical trial of SUP versus placebo in infants admitted to the CICU. The study investigators hypothesize that a priori feasibility measures will be achieved during the study period. Primary Aim 2 of the study is to examine the differences of UGI bleeding in critically ill infants with CHD receiving SUP versus those receiving placebo. The study investigators hypothesize that the rate of UGI bleeding will be no different between infants exposed to SUP and to placebo. Secondary Aim 1 of the study is to compare the differences in the abundance of microbial taxa and functional profiles of the aerodigestive tract microbiome between infants receiving SUP and those receiving placebo and before/after the start of SUP. The study investigators hypothesize that there will be significant differences in the abundance of microbial taxa and the functional profiles between the 2 groups - with a more favorable microbial profile present in infants in the placebo group. Secondary Aim 2 is to examine the difference in the incidence of hospital-acquired infections in critically ill infants with CHD receiving SUP versus placebo. The study investigators hypothesize the rate of hospital-acquired infections will be higher in patients exposed to SUP when compared to placebo.
Study Design & Methods. A single-center, prospective, double-blinded, randomized, controlled trial will be conducted as a feasibility study for a larger multicenter trial. Consecutive infants < 12 months of age with CHD admitted to the CICU and anticipated to require respiratory support for > 24 hours will be enrolled and randomized to receive a histamine-2 receptor antagonist (H2RA) medication or study placebo. Patients will remain in the study until discontinuation of respiratory support, discharge from the CICU or study day 14. Oral, gastric and stool samples will be obtained prior to receiving the first dose of study drug and subsequently at the end of the study. The samples will be analyzed for 16S RNA and metagenomic shotgun sequencing for microbiome composition. Gastric pH will be recorded on all gastric samples. Demographics, nutrition variables, medications, and respiratory data will be collected for all patients while enrolled in the study. An independent Drug Safety and Monitoring Board (DSMB) will monitor patient safety every 6 months and after any significant adverse event.
Outcomes. The primary outcomes will be study feasibility and incidence of clinically significant UGI bleeding. Feasibility will be defined as: 1) > 80% screening of eligible patients, 2) > 20% consent rate, 3) > 80% receive timely first dose of study drug, and 4) > 80% protocol adherence. Clinically significant UGI bleeding will be defined as new-onset bleeding with subsequent pre-defined physiologic or hemodynamic changes. The secondary outcomes of the study will be observed differences in the aerodigestive microbial diversity between study groups, mortality, length of stay, duration of respiratory support, bleeding events, incidence of necrotizing enterocolitis and incidence of hospital-acquired infections (ventilator-associated pneumonia, central line-associated bloodstream infections, catheter-associated urinary tract infections, superficial sternal infection or mediastinitis).
Study Type
Enrollment (Actual)
Phase
- Phase 4
Contacts and Locations
Study Locations
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Massachusetts
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Boston, Massachusetts, United States, 02115
- Boston Children's Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- < 12 months of age (including premature newborns),
- diagnosed with congenital heart disease (including anatomic, myopathic and arrhythmic conditions),
- received ≤ 1 dose of SUP (including histamine-2 receptor antagonists, proton pump inhibitors, and sucralfate) during current admission, AND
- anticipated to require respiratory support for > 24 hours during their CICU stay. Respiratory support includes mechanical ventilation, non-invasive positive-pressure ventilation and high-flow oxygen therapy.
Exclusion Criteria:
- prior use of antacids (including histamine-2 receptor antagonists, proton pump inhibitors, or sucralfate) in the past month for > 7 days,
- active gastrointestinal bleeding,
- active Helicobacter pylori infection,
- administration of high-dose steroids (equivalent dosing to 15 mg/kg/day of methylprednisolone),
- will receive ketorolac (intravenous nonsteroidal anti-inflammatory drug) during admission,
- exposed to specific anticoagulants (high-dose aspirin, direct thrombin inhibitors and GPIIbIIIa inhibitors),
- planned to undergo or recently has undergone gastrointestinal surgery (i.e. repair of duodenal atresia)
- supported by extracorporeal membrane oxygenator (ECMO) or ventricular assist device (VAD),
- currently enrolled in another intervention trial,
- known to be allergic to H2RAs,
- admitted for palliative care,
- prior enrollment in the study, OR
- primary provider declines enrollment.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: QUADRUPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
PLACEBO_COMPARATOR: Placebo
Subjects randomized to placebo will receive an equivalent volume (mL) of normal saline intravenously or Ora-plus orally based on weight and age.
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Patients will be randomized to either receive a placebo or famotidine (study drug).
Other Names:
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ACTIVE_COMPARATOR: Study Drug
Subjects randomized to study drug will receive famotidine, a histamine-2 receptor antagonist.
Dosing will be weight based and age-dependent.
Infants < 90 days old will receive either 0.5mg/kg intravenously daily or 0.5mg/kg orally twice a day of famotidine.
Infants ≥ 90 days or older will receive 0.25mg/kg intravenously every 12 hours or 0.5mg/kg orally twice a day.
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Patients will be randomized to either receive a placebo or famotidine (study drug).
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Predefined Feasibility Outcomes to Assess Trial Success
Time Frame: Through study completion, anticipated 2 years.
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Feasibility will be defined by the following metrics: (1) if >80% of eligible patients are approached for consent (screening), (2) >20% of eligible patients are randomized (consent and enrollment), (3) >80% of enrolled patients received first dose of study drug within 48 hours (allocation), and (4) >80% compliance to protocol and treatment group (protocol adherence).
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Through study completion, anticipated 2 years.
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Rate of upper gastrointestinal bleeds
Time Frame: Through study completion, anticipated 2 years.
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To examine the difference in the incidence of clinically significant upper gastrointestinal (UGI) bleeding in critically ill infants with CHD receiving SUP versus placebo to demonstrate safety.
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Through study completion, anticipated 2 years.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Microbiome alterations
Time Frame: Through study completion, anticipated 2 years.
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To compare the absolute and serial differences in the abundance of bacteria and functional microbial profiles in the aerodigestive tract between critically ill infants with CHD receiving SUP compared to placebo.
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Through study completion, anticipated 2 years.
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Rate of hospital-acquired infections
Time Frame: Through study completion, anticipated 2 years.
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To examine the difference in the incidence of hospital-acquired infections in critically ill infants with CHD receiving SUP versus placebo.
Hospital-acquired infections include ventilator-associated pneumonia, central line-associated bloodstream infections, catheter-associated urinary tract infections, superficial sternal infection, or mediastinitis.
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Through study completion, anticipated 2 years.
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Kimberly I Mills, MD, Boston Children's Hospital
- Principal Investigator: Ben D Albert, MD, Boston Children's Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Digestive System Diseases
- Pathologic Processes
- Cardiovascular Diseases
- Congenital Abnormalities
- Gastrointestinal Diseases
- Hemorrhage
- Cardiovascular Abnormalities
- Heart Diseases
- Ulcer
- Heart Defects, Congenital
- Gastrointestinal Hemorrhage
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Gastrointestinal Agents
- Anti-Ulcer Agents
- Histamine Antagonists
- Histamine Agents
- Histamine H2 Antagonists
- Famotidine
Other Study ID Numbers
- IRB-P00028715
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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