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Clinical Trial Summary

The study primary objective is to compare the clinical efficacy of two formulations in the supportive treatment of lactose intolerance.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01145339
Study type Interventional
Source Eurofarma Laboratorios S.A.
Contact
Status Completed
Phase Phase 3
Start date July 2011
Completion date March 2012