CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 12 enrolled
Drug / intervention
32ppm Silver Particle +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01405794
NCT01405794Phase 2Completed

In-Vivo Assessment of Silver Biomaterial Nano-Toxicity 32 Ppm

University of Utah·interventional·Posted Jul 29, 2011·Updated Jul 4, 2016

In Brief

A Phase 2 clinical trial evaluating 32ppm Silver Particle and Placebo for Healthy. Completed, enrolled 12 participants across 1 site.

Detailed Summary

The investigators propose to study oral commercial silver nanoparticle products on human enzyme activity.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedJul 29, 2011
Enrollment StartJul 1, 2011
Primary CompletionNov 1, 2011
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 14.9 years ago

Interventions

32ppm Silver Particledrug

Oral silver dose of 32ppm

Placebodrug

Sterile Water No Silver