Trials / Unknown
UnknownNCT03598010
Safety, Tolerability and Preliminary Efficacy of Lenodiar Pediatric in Diarrhea
Safety, Tolerability and Preliminary Efficacy of Oral Administration of Tannins and Flavonoids in the Management of Pediatric Diarrhea
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 240 (estimated)
- Sponsor
- Aboca Spa Societa' Agricola · Industry
- Sex
- All
- Age
- 1 Year – 12 Years
- Healthy volunteers
- Not accepted
Summary
Evaluation of the efficacy of a treatment with Actitan-F, a natural molecular complex of tannins (from Agrimony and Tormentil) and flavonoids (Chamomile) in a pediatric population of children affected by acture/prolonged/chronic diarrhea
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Actitan-F (7dd) | 1 sack every 4 hours, maximum 4 sacks/day for 7 days. |
| DEVICE | Actitan-F (28dd) | 1 sack every 4 hours, maximum 4 sacks/day for 28 days. |
Timeline
- Start date
- 2019-10-01
- Primary completion
- 2020-12-01
- Completion
- 2021-03-01
- First posted
- 2018-07-26
- Last updated
- 2019-06-04
Source: ClinicalTrials.gov record NCT03598010. Inclusion in this directory is not an endorsement.