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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01809951
Other study ID # ANID-1101
Secondary ID
Status Completed
Phase N/A
First received January 25, 2013
Last updated June 14, 2017
Start date August 2011
Est. completion date July 2013

Study information

Verified date June 2017
Source Indonesia University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The use of soy-isolate protein based formula for infants with cow's milk protein intolerance is common in Indonesia, however, there has not been any systematic collection of clinical data to determine the formula's gastrointestinal tolerance, and the parent's perceptions regarding the formula.


Recruitment information / eligibility

Status Completed
Enrollment 534
Est. completion date July 2013
Est. primary completion date April 2013
Accepts healthy volunteers No
Gender All
Age group 6 Months to 12 Months
Eligibility Inclusion Criteria:

- infants of 6 - 12 months of age

- full term infants

- birth weight more than 2500 grams

- infants developed symptoms suggestive adverse reactions to cow's milk protein in the investigator's clinical judgements

- subject is prescribed a soy-based infant formula by physician

Exclusion Criteria:

- established/suspected hypersensitivity fo soy

- presence of adverse reactions to cow's milk caused by coincidental infections or other systemic disease

- history of blood group incompatibility, premature delivery, HIV infections, major congenital abnormalities, systemic diseases

- presence of severe gastrointestinal disorder

- subject is participating in any interventional clinical study

Study Design


Locations

Country Name City State
Indonesia Divisi Alergi Imunologi FKUI RSCM Jakarta

Sponsors (1)

Lead Sponsor Collaborator
Melva Louisa

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Parent's acceptance in the feeding of a soy-based infant formula with LCP in infants with symptoms suggestive adverse reactions to cow milk protein 4-week
Secondary percentage of infants with gastrointestinal adverse events 4-week
Secondary percentage of infants with adverse events 4-week
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