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The Effects of a High-fiber Formula in Children With Failure to Thrive

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Abbott

Status

Completed

Conditions

GI Tolerance

Treatments

Other: pediatric formula

Study type

Observational

Funder types

Industry

Identifiers

NCT02819401
ANTK1001

Details and patient eligibility

About

The present study is designed to determine the gastrointestinal tolerability of enteral nutritional products, physicians and parents' overall perception of enteral nutrition products as well as providing basic demographic information on pediatric populations prescribed these formula for supportive treatment as part of the routine healthcare service in Turkey.

Enrollment

345 patients

Sex

All

Ages

1 to 10 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age; 1-10 years (inclusive)
  • Children diagnosed as failure-to-thrive(FTT).
  • Children who have been recently prescribed and treatment initiated with isocaloric or hypercaloric high-fiber pediatric enteral formula suitable for oral and/or nasogastric tube feeding before inclusion in the study.

Exclusion criteria

  • Chronic renal disorder
  • Decompensated liver disease
  • Any other chronic condition that was not under control (e.g. diabetes, thyroid disorder, etc.)
  • Any type of malignant disease including leukemia and lymphoma
  • Cystic fibrosis
  • Short bowel syndrome
  • Any type of food allergy or intolerance
  • Growth hormone deficiency
  • Use of enteral feeding within the last 4 weeks

Trial contacts and locations

17

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Data sourced from clinicaltrials.gov

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