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Clinical Trial Summary

The aim of the study is to assess the effectiveness of this new formula on regurgitations and secondarily its effect on digestive tolerance through a randomized, controlled, double-blind trial against a comparator.


Clinical Trial Description

The study duration is 1 month and 2 days. It is possible to add 2 additional months (optional).

The 2 first days (from D-3 to D0) correspond to the pre-selection period. These 2 days are followed by the follow-up month (from D0 to D30). It is possible to add an optional follow up of 2 months (form D30 to D90). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04358146
Study type Interventional
Source United Pharmaceuticals
Contact Bastian CUMINAL
Phone 0033155372222
Email b.cuminal@novalac.com
Status Not yet recruiting
Phase N/A
Start date July 1, 2020
Completion date March 1, 2022