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CompletedNCT00682955ZincUpdated May 23, 2008

Comparing the Efficacy of Different Zinc Formulations in the Treatment of Diarrhea

An interventional study of Zinc Sulphate and Zinc Sulphate in Incidence of Acute Diarrhea and Incidence of Abdominal Pain, sponsored by Aga Khan University. Completed at 2 sites in Pakistan. Open to participants aged 6 Months to 5 Years. Per ClinicalTrials.gov, last updated 2008-05-23.

Sponsored by Aga Khan University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Non-randomized
Ages
6 Months to 5 Years
Sex
All
01

Study summary

This project is aimed to evaluate the efficacy of two different zinc formulations (dispersible Zinc tablets versus Zinc suspension) for the treatment of acute diarrhea in hospital based settings. Additionally we intend to compare the effectiveness of treatments of different groups on the basis of usage of Zinc in the treatment of diarrhoea, and to monitor additional treatment components such as ORS, antibiotic usage rates.

Read the detailed description

This will be an open randomized trial in children designed to measure the impact and efficacy of daily zinc administration. There will be two groups in the study, one group will receive Zinc in the form tablets, other will receive in the form of suspension, both of these groups will also receive recommended treatment of diarrhea as per WHO protocol and these groups will be enrolled from the patients admitting in the Paediatric Unit of Civil Hospital, Hyderabad and NICH, Karachi with the complain of acute diarrhoea.

The intervention study will be undertaken in hospital based settings. A total recruitment of 300(150 each in each group) has been targetted during the study duration. The duration of this study shall be 9 months.

A brief history will be taken regarding the current illness and will be noted down in the specific forms. After the history the patient will be completely examined by the duty doctors, examination will emphasize of the vitals, status of dehydration and anthropometry. Patient will then be randomized in one of the groups and the procedure of using Zinc tablets or suspension will be explained to the mother or caretaker.The patient will be advised treatment according to the general condition and state of the dehydration and general health. All treatments will be noted down in the specific forms to have a record of what have been given to the patient and to keep the record of fluid intake. Stool samples for the detailed report and culture and sensitivity will be collected \& sent to have the information regarding the status of stool and any isolated organism.

Follow-ups

  • The patients will be followed \& examined thoroughly every 8 hourly till the time of discharge by a trained RMO.
  • At each follow up, details of illness characteristics, including the number and character of stools and vomiting, will be obtained.
  • Information regarding the associated symptoms including fever, abdominal pain distension and dysentery will be obtained. Hydration status, vitals and weight will also be assessed.
  • RMO will record about the proper dosages of zinc and confirm that weather or not patient is taking his medications during every follow up
  • RMO will also document the recovery of diarrhea in terms of reduction in frequency and duration of diarrhoea and all the information will be noted in the assigned follow up forms.
  • Any adverse effect of the associated with the Zinc will also be recorded.
  • Compliance will be measured by reported intake and by measuring the remaining volume of syrup in the returned bottles and number of tablets used in the blisters.
  • At the time of discharge a discharge summary form is also filled by RMO
  • The patients who will be discharged will be followed at home for a total of two weeks of illness.
02

Conditions studied

  • Incidence of Acute Diarrhea
  • Incidence of Abdominal Pain

Keywords

  • Diarrhea
  • Zinc Sulphate
  • Efficacy
03

In context

Diarrhea

852 studies on the registry are indexed under Diarrhea; 78 are open to participants now.

This study's enrollment of 300 is above the median of 136 across 713 interventional studies indexed under Diarrhea.

Browse Diarrhea studies →

Lead sponsor

Aga Khan University is the lead sponsor of 290 studies on the registry; 44 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Months to 5 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Children 6 months to 5 years of age
  • Presented with passage of 3 or more loose or watery stools
  • Caretakers are willing to let their child to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Failure to produce consent.
  • Children with severe malnutrition or having chronic illness
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (actual)

Study arms

  • Active comparator
    B

    This group has been given Zinc Sulphate in Suspension Form.

    Drug: Zinc Sulphate

  • Active comparator
    A

    This group has been given Tablets of Zinc Sulphate.

    Drug: Zinc Sulphate

Interventions

  • DrugZinc Sulphate

    20 mg per day, Zinc Sulphate tablet has been given to subjects.

    Also known as: Zincol

  • DrugZinc Sulphate

    20 mg per day of Zinc Sulphate in suspension form has been given to subjects.

    Also known as: Zincat

06

What researchers measure

Primary outcomes

  1. Comparison of Efficacy of the two different Zinc Sulphate formulations

    Time frame: 9 months

Secondary outcomes

  1. Comparison of side effects of the two different Zinc Sulphate formulations used

    Time frame: 9 months

07

Study locations

2 sites
  • Civil Hospital
    Hyderabad, Sindh 75300, Pakistan
  • National Institute of Child Health
    Karachi, Sindh 75300, Pakistan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 23, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00682955
Lead sponsor
Aga Khan University
Collaborators
Civil Hospital, Hyderabad, Pakistan, National Institute of Child Health, Karachi, Pakistan
First posted
May 23, 2008
Start date
Aug 2007
Primary completion
Apr 2008
Completion
Apr 2008
Last update
May 23, 2008

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2008. You cannot join it, but the record below documents what was studied.

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