WHO ICTRP trial

Safety evaluation of Uniform Particle NovaSil in Children (Phase I study)

PACTR201311000711179 · Pan African Clinical Trials Registry (PACTR) · Not Recruiting

Key facts

Trial ID PACTR201311000711179
Public title Safety evaluation of Uniform Particle NovaSil in Children (Phase I study)
Scientific title Enterosorbent Intervention Therapies for Populations at risk of Aflatoxin-Related Diseases: Safety evaluation of Unifrom Particle NovaSil in Children (Phase I)
Primary sponsor Noguchi Memorial Institute for Medical Research
Secondary sponsors Texas A&M University
Registry Pan African Clinical Trials Registry (PACTR)
Recruitment status Not Recruiting
Study type Interventional
Phase Not Applicable
Countries Ghana;Ghana;Ghana;Ghana;Ghana;Ghana
Conditions Injury, Occupational Diseases, Poisoning Paediatrics Aflatoxin exposure;Injury, Occupational Diseases, Poisoning;Paediatrics;Aflatoxin exposure
Interventions Unifrom Particle Size NovaSil (UPSN) ;Unifrom Particle Size NovaSil (UPSN) ;Placebo
Registration date Nov 22, 2013
Target size 75
Secondary IDs not applicable
Registry page pactr.samrc.ac.za

At a glance

  • No Results available

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

Browse all WHO ICTRP trial registrations