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Oral Zinc for the Treatment of Acute Diarrhea in US Children

Primary Purpose

Diarrhea, Gastroenteritis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Zinc Sulfate
Placebo oral capsule
Sponsored by
Boston Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diarrhea focused on measuring Diarrhea, Gastroenteritis, Zinc Supplementation

Eligibility Criteria

6 Months - 6 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Healthy Children with non-bloody diarrhea illness defined as loose or watery stools
  • Symptoms must be present for greater than 24 hours but less than 72 hours.
  • Comorbid conditions including; Asthma, Gastroesophageal reflux (unless followed by a Gastroenterologist), Mild speech, language, motor delays, Benign heart murmurs, Isolated atrial septal defect (ASD) or ventricular septal defect (VSD), Epilepsy (unless developmentally delayed), Children born Prematurely between 33-37 weeks without long term sequelae, Repaired tetralogy of fallot (no cardiac issues for >6 months), Diabetes may be enrolled in the study.

Exclusion Criteria:

  • Children with symptoms less than 24 hours
  • Children with symptoms greater than 24 hours
  • Failure to thrive
  • G or J tube
  • Major surgery within last 3 months
  • Minor surgery (tonsillectomy, ear tubes, skin lesion removals etc) within last 1 month
  • Followed by GI service for any reason (crohns, ulcerative colitis, constipation)
  • Developmental delay, patient >1 year behind milestones
  • Current brain tumor
  • Currently being treated for cancer or in remission < 6 months
  • Intussuception
  • Antibiotics in the last 14 days or currently taking antibiotics for any reason
  • Autism
  • Children born premature <33 weeks
  • Cystic Fibrosis
  • Major congenital Heart Disease (any disease where child's baseline oxygen saturations <93%)
  • Short Gut
  • Liver disease
  • History of bowel resection

Sites / Locations

  • Children's Hospital Boston

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Placebo Comparator

Placebo Comparator

Arm Label

Outpatient Zinc Sulfate

Inpatient Zinc Sulfate

Outpatient Placebo

Inpatient Placebo

Arm Description

Zinc Sulfate

Zinc Sulfate

Placebo oral capsule

Placebo oral capsule

Outcomes

Primary Outcome Measures

Duration of Diarrhea in Acute Diarrheal Illnesses in a Developed Nation While Taking Zinc or Placebo.
Patients symptoms will be assessed to identify the duration of diarrhea between zinc and placebo groups before it becomes chronic diarrhea which by definition lasts longer than 14 days. Outcome of all patients in study will be assessed at study conclusion.

Secondary Outcome Measures

Examine the Potential Cost Benefits of Supplementation With Zinc in Reducing Number of Daycare Days Not Attended and Work Days Lost by Parents
Assess Parent Reporting Reliability Comparing Survey Responses to Phone Interview.
Kappa inter-rater reliability measurement was done to analyze the agreement between the phone call data with parents reporting the number of episodes of diarrhea per day were compared to the written symptom charts where parents recorded the number of episodes of diarrhea per day. The inter-rater reliability ranges from 0 to 1 with scores of 0-0.2 = poor agreement, 0.2-0.4 = fair agreement, 0.4-0.6 = moderate agreement, 0.6-0.8 = good agreement and 0.8-1 = very good agreement

Full Information

First Posted
September 2, 2010
Last Updated
August 18, 2018
Sponsor
Boston Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01198587
Brief Title
Oral Zinc for the Treatment of Acute Diarrhea in US Children
Official Title
A Double Blind Randomized Placebo Controlled Trial of Oral Zinc for Children With Acute Diarrhea in a Developed Nation.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
November 2010 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
June 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston Children's Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Diarrheal diseases are the third leading cause of mortality in the world, with nearly 2 million deaths annually among children under age 5 years. Several clinical trials of oral zinc supplementation performed in developing country populations have confirmed this nutrient's efficacy in reducing the severity and frequency of diarrhea. The World Health Organization (WHO) has recommended global use of zinc supplementation in all children with diarrhea despite little or no data from trials in industrialized/developed settings. In the United States over 4 million children suffer annually from diarrheal illness. Although mortality is not a significant factor in U.S. cases, 75% of all cases present to medical care resulting in over 200,000 hospitalizations annually for diarrhea. This has significant impact on U.S. healthcare costs, with an average of $391 per outpatient treatment and $2,549 per inpatient treatment spent on each episode of acute diarrheal illness. The goal of this study is to evaluate the effectiveness of oral zinc in decreasing the duration of diarrhea in children treated as outpatients and in decreasing the duration of hospitalization in children treated as inpatients in an industrialized country. The results of this study promise to have a substantial impact on the management of a common pediatric health problem, and could conceivably affect direct and indirect healthcare costs to society.
Detailed Description
In developing countries, diarrheal diseases are a leading cause of childhood morbidity and mortality. In the United States an estimated 4.67 million children per year suffer from gastroenteritis with a diarrheal component, impacting the delivery and cost of healthcare. Seventy-five percent of these children are brought to physician care across a range of settings from clinics to emergency departments. Children less than five years of age average 1.3 - 2.5 episodes per year, with 1.4% of those children requiring hospitalization annually. This results in an estimated 209,000 hospitalizations yearly for gastroenteritis. The impact of acute gastrointestinal disease can be felt in the developed world, including the United States, as cost attributed to hospitalization and productivity lost. Attempts at treating gastroenteritis have included Oral Rehydration Solution (ORS), introduced 30 years ago by the WHO, which continues to provide a safe and effective way to maintain hydration during acute illness. ORS, however, does not reduce the volume or frequency of stool output in diarrhea. The anti-diarrheal medication loperamide (Imodium®) was commonly used in children until reports of serious adverse reactions caused its use to fall out of favor. There are no other medications or supplements available to specifically treat the diarrheal component of gastroenteritis and studies have shown that adherence to treatment recommendations regarding fluid therapy is poor because care givers want to reduce duration of illness as opposed to supporting children through the natural course of the disease. The desire to relieve diarrheal symptoms often leads care givers to seek antibiotics during a time of rising antibiotic resistance, as well as other treatments with no proven efficacy. Zinc is an essential trace element for humans. Its physiologic roles are seen throughout the body as a critical cofactor for enzymatic reactions; most notable are its actions in the gastrointestinal (GI) tract. Zinc is an important component of brush border enzymatic activity which promotes gastrointestinal absorption, it regulates water/electrolyte transport at the cellular level, and it enhances the repair of the intestinal mucosa by bolstering immune function. Over the past 10-15 years, there have been more than a dozen randomized controlled trials of zinc supplementation performed in children living in developing countries that have reported improvements in the duration and severity of diarrhea when compared to placebo in a variety of in- and outpatient settings. The majority of zinc trials were conducted in countries at high risk of zinc deficiency, but those conducted at medium risk showed similar effect on duration and severity. When stratified across all nutritional groups based on serum zinc levels a significant effect was seen compared to placebo despite baseline zinc level, with no occurrence of serious adverse reaction in any group. Given these results, the WHO has endorsed zinc supplementation for all children with acute diarrhea, despite the lack of data from similarly designed studies in industrialized/developed settings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea, Gastroenteritis
Keywords
Diarrhea, Gastroenteritis, Zinc Supplementation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
71 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Outpatient Zinc Sulfate
Arm Type
Experimental
Arm Description
Zinc Sulfate
Arm Title
Inpatient Zinc Sulfate
Arm Type
Experimental
Arm Description
Zinc Sulfate
Arm Title
Outpatient Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo oral capsule
Arm Title
Inpatient Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo oral capsule
Intervention Type
Drug
Intervention Name(s)
Zinc Sulfate
Other Intervention Name(s)
Treatment
Intervention Description
For children ages 6month to 1 year, 12.5mg orally daily for 14 days mixed in 60 mL of fluid. For children aged 1 year and above 25mg orally daily for 14 days mixed in 60 mL of fluid.
Intervention Type
Drug
Intervention Name(s)
Placebo oral capsule
Other Intervention Name(s)
Placebo
Intervention Description
Effervescent oral capsules with similar taste to treatment drug Zinc Sulfate is provided to each patient randomized to the placebo arms of the study
Primary Outcome Measure Information:
Title
Duration of Diarrhea in Acute Diarrheal Illnesses in a Developed Nation While Taking Zinc or Placebo.
Description
Patients symptoms will be assessed to identify the duration of diarrhea between zinc and placebo groups before it becomes chronic diarrhea which by definition lasts longer than 14 days. Outcome of all patients in study will be assessed at study conclusion.
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Examine the Potential Cost Benefits of Supplementation With Zinc in Reducing Number of Daycare Days Not Attended and Work Days Lost by Parents
Time Frame
over the 14 day symptom monitoring period
Title
Assess Parent Reporting Reliability Comparing Survey Responses to Phone Interview.
Description
Kappa inter-rater reliability measurement was done to analyze the agreement between the phone call data with parents reporting the number of episodes of diarrhea per day were compared to the written symptom charts where parents recorded the number of episodes of diarrhea per day. The inter-rater reliability ranges from 0 to 1 with scores of 0-0.2 = poor agreement, 0.2-0.4 = fair agreement, 0.4-0.6 = moderate agreement, 0.6-0.8 = good agreement and 0.8-1 = very good agreement
Time Frame
agreement over the 14 day follow up period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Healthy Children with non-bloody diarrhea illness defined as loose or watery stools Symptoms must be present for greater than 24 hours but less than 72 hours. Comorbid conditions including; Asthma, Gastroesophageal reflux (unless followed by a Gastroenterologist), Mild speech, language, motor delays, Benign heart murmurs, Isolated atrial septal defect (ASD) or ventricular septal defect (VSD), Epilepsy (unless developmentally delayed), Children born Prematurely between 33-37 weeks without long term sequelae, Repaired tetralogy of fallot (no cardiac issues for >6 months), Diabetes may be enrolled in the study. Exclusion Criteria: Children with symptoms less than 24 hours Children with symptoms greater than 24 hours Failure to thrive G or J tube Major surgery within last 3 months Minor surgery (tonsillectomy, ear tubes, skin lesion removals etc) within last 1 month Followed by GI service for any reason (crohns, ulcerative colitis, constipation) Developmental delay, patient >1 year behind milestones Current brain tumor Currently being treated for cancer or in remission < 6 months Intussuception Antibiotics in the last 14 days or currently taking antibiotics for any reason Autism Children born premature <33 weeks Cystic Fibrosis Major congenital Heart Disease (any disease where child's baseline oxygen saturations <93%) Short Gut Liver disease History of bowel resection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michelle L Niescierenko, MD
Organizational Affiliation
Boston Children's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Richard Bachur, MD
Organizational Affiliation
Boston Children's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christopher Duggan, MD, MPH
Organizational Affiliation
Boston Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital Boston
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

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Oral Zinc for the Treatment of Acute Diarrhea in US Children

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