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Completed

NCT Number: NCT00198666

Efficacy of Zinc in the Treatment of Pneumonia

This study is designed to evaluate the efficacy of zinc supplementation in the treatment of children under the age of two years who have been hospitalized with severe pneumonia.

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Key information

Age range

Up to 23 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

This study was a randomized, double-blind, placebo-controlled clinical trial conducted between September 2003 and August 2004 at the Christian Medical College (CMC) Hospital in Vellore, India. CMC Hospital is a large teaching hospital and medical center that is accessed directly by the population of Vellore and adjoining districts and by referrals from local medical practitioners.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • children under two years old hospitalized with Pneumonia

Exclusion criteria

  • healthy children

Treatment and study plan

Zinc

Drug

Elemental Zinc

Primary outcomes

  1. Duration of severe symptoms

    Time frame: 2 years

Secondary outcomes

  1. Time to recovery from severe pneumonia

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Johns Hopkins Bloomberg School of Public Health

Other

Registry information

Official study title

Efficacy of Zinc in the Treatment of Pneumonia in Hospitalized Children Less Than 2 Years of Age

Important dates

Study start
2003
Primary completion
2004
Study completion
2004
First posted
Sep 20, 2005
Registry last updated
Jan 12, 2015

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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