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Completed

NCT Number: NCT03078842

Zinc Dosing Trial - Does Dose Reduction Reduce Side Effects But Retain Efficacy in Diarrhoea Management

Diarrhoea continues to be a major cause of child deaths. Current treatment of acute watery diarrhoea includes oral rehydration solution (ORS), zinc and continued feeding. The use of zinc is based on a number of studies that showed that zinc reduces the duration and severity of diarrhoea. The recommended dose of zinc in 6-59 month old children is 20mg/day for 10-14 days. This dose is associated with an increased risk of vomiting. No dosing studies are available to determine the optimal dose of zinc, which while maintaining the benefits also has a low risk of vomiting.

The investigators will conduct a double-blind randomized controlled trial of three doses of zinc (20mg/day, 10mg/day and 5mg/day) in two settings - one in Sub-Saharan Africa and the other in South Asia. The study population will be 4500 children with diarrhoea of less than 72 hours duration who are aged 6-59 months. They will be recruited from outpatient health facilities. All enrolled children will receive ORS and continued feeding as recommended by the World Health Organization. Those allocated to the standard zinc dose will receive an oral dispersible tablet with 20mg zinc daily for 14 days. Those allocated to lower dose zinc will receive identical tablets with either 10mg or 5mg zinc daily for 14 days. Enrolled children will be followed by until recovery from diarrhoea or 15 days after enrolment, whichever is later. In addition, study children will be assessed again at thirty (30), forty-five (45), and sixty (60) days to estimate impact on post illness outcomes. Primary outcomes will be mean duration of diarrhoea, proportion of episodes that last longer than 5 days, mean number of stools and proportion of children with vomiting.

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Key information

Age range

6 month–59 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre for Public Health Kinetics, New Delhi, India

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 6 to 59 completed months of age
  • Acute diarrhoea of less than 3 days at the time of screening or dysentery, defined as visible blood in the stool, of less than 3 days at the time of screening
  • Likely to stay within the study area for the next 2 months
  • Written informed consent from caretaker

Exclusion criteria

  • Presence of severe acute malnutrition (WHZ<-3 or oedema)
  • Presence of severe dehydration that cannot be corrected in 4 to 6 hours
  • Signs of severe pneumonia (WHO definition of pneumonia with danger signs), sepsis, rapid diagnostic test (RDT) -confirmed malaria or other severe illness
  • Previously or currently enrolled in the study
  • Currently enrolled in another study
  • Other child currently enrolled in the study in the same household
  • Not intending to remain in study area for the duration of the study
  • Parents refuse participation in the study

Treatment and study plan

Zinc tablets, 20 mg per day

Dietary Supplement

Participants will receive rehydration, dietary counseling, and 1 tablet per day for 14 days of zinc-tablets, each of which contains 20 mg of zinc

Zinc tablets, 10 mg per day

Dietary Supplement

Participants will receive rehydration, dietary counseling, and 1 tablet per day for 14 days of zinc-tablets, each of which contains 10 mg of zinc

Zinc tablets, 5 mg per day

Dietary Supplement

Participants will receive rehydration, dietary counseling, and 1 tablet per day for 14 days of zinc-tablets, each of which contains 5 mg of zinc

Primary outcomes

  1. Proportion with long duration of diarrhoea

    Time frame: Measured daily for 15 days

    Diarrhoea continuing beyond five days

  2. Continuation of diarrhoea symptoms

    Time frame: Measured daily for 15 days

    Total number of loose or watery stools after enrolment

  3. Proportion of children vomiting after zinc treatment

    Time frame: Measured daily for 15 days

    Vomiting within 30 minutes of administration of zinc tablet

Secondary outcomes

  1. Proportion of children experiencing serious adverse events (SAEs)

    Time frame: Measured until 60 days

    Serious adverse events (life-threatening or requiring hospitalization)

  2. Proportion with intermediate duration of diarrhoea

    Time frame: Measured daily for 15 days

    Diarrhoea continuing beyond three days

  3. Proportion of guardians with positive attitude towards treatment

    Time frame: Day 15

    The guardians will be asked if was easy to administer the treatment, if they think the child liked the treatment, if they saw any changes in the children after the treatment and if they would recommend this treatment to their friends' children.

  4. Treatment adherence

    Time frame: Measured daily for 15 days

    Mean number of tablets consumed by the study child during the 14 day treatment period.

  5. Mean serum plasma zinc concentration at Days 1, 3, 7, 15, 21 and 30

    Time frame: Days 1, 3, 7, 15, 21 and 30

    Mean serum plasma zinc concentration at Days 1, 3, 7, 15, 21 and 30

  6. Illness symptoms between day 15 and 60 after the treatment

    Time frame: Days 30, 45, 60

    2-week period prevalence and number of days with diarrhoea, fever, or respiratory symptoms

Sponsors and collaborators

Lead sponsor

Ayesha De Costa

Other

Collaborators

  • Boston Children's Hospital
  • Center for Public Health Kinetics
  • Muhimbili University of Health and Allied Sciences

Registry information

Official study title

Establishing the Optimal Dose of Therapeutic Zinc Supplementation for the Treatment of Acute Diarrhea in Under Five Children - a Dose Response Trial in a South Asian and a Sub-Saharan African Setting

Acronym: ZTDT

Important dates

Study start
2017
Primary completion
2019
Study completion
2020
First posted
Mar 13, 2017
Registry last updated
Oct 8, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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