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Soy-based Formula
3: Soy formula for Newborns
Phase 2 & 3
Waitlist Available
Research Sponsored by Abbott Nutrition
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 35 days
Awards & highlights
Study Summary
The objective of this study is to assess the comparative gastrointestinal (GI) tolerance of normal term infants to two experimental soy-based formulas, relative to a commercially available soy-based formula.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 35 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~35 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Gastrointestinal tolerance from Study Visit 1 to Study Visit 3 at 35 days of age.
Secondary outcome measures
Additional gastrointestinal measures of tolerance from Study Visit 1 to Study Visit 3 at 35 days of age
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: 3: Soy formulaExperimental Treatment1 Intervention
experimental soy formula #2
Group II: 1: Soy formulaExperimental Treatment1 Intervention
experimental soy formula #1
Group III: 2: Soy FormulaActive Control1 Intervention
Commercially available soy formula
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Who is running the clinical trial?
Abbott NutritionLead Sponsor
168 Previous Clinical Trials
33,350 Total Patients Enrolled
John Lasekan, PhDStudy ChairAbbott Nutrition
3 Previous Clinical Trials
158 Total Patients Enrolled
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