CClinicalTrials.gg
CompletedNCT00076375Updated Jun 24, 2005

Preliminary Study of Safety and Efficacy of Nanocrystalline Silver Cream in Atopic Dermatitis (Eczema)

A Phase 2 interventional study of Nanocrystalline silver cream (NPI) in Atopic Dermatitis and Eczema, sponsored by Nucryst Pharmaceuticals. Completed at 19 sites in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2005-06-24.

Sponsored by Nucryst Pharmaceuticals · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
180
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Nanocrystalline silver (very small particles of silver) is the active ingredient in Acticoat dressings, which have been approved for the treatment of burns and other wounds. Silver has been used for decades as an effective antimicrobial agent. In animal studies, nanocrystalline silver cream (NPI) has also demonstrated anti-inflammatory activity. Thus, nanocrystalline silver cream is being evaluated in the treatment of inflammatory skin conditions such as atopic dermatitis (eczema).

Approximately 180 study subjects with a definitive diagnosis of mild to moderate eczema will be enrolled in this study. Subjects will be randomly assigned to treatment with placebo, 0.5% NPI or 1% NPI for the 6-week treatment period. Assessments of treatment effect and safety will be performed weekly. Upon completion of the study, subjects may be eligible for 12 weeks of open-label treatment with 1% NPI.

02

Conditions studied

  • Atopic Dermatitis
  • Eczema

Keywords

  • Atopic Dermatitis
  • Eczema
03

In context

Dermatitis, Atopic

1,419 studies on the registry are indexed under Dermatitis, Atopic; 258 are open to participants now.

This study's enrollment of 180 is above the median of 83 across 1,125 interventional studies indexed under Dermatitis, Atopic.

Browse Dermatitis, Atopic studies →

Lead sponsor

This is the only study on the registry with Nucryst Pharmaceuticals as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

  • Male or female, any race, 18 to 65 years of age.
  • Females must be post-menopausal, surgically sterile, or if of child-bearing potential, not pregnant (confirmed by test) and using an adequate method of birth control.
  • Subjects must have eczema that covers a minimum of 5% total body surface area.
  • Subjects must agree not to use other eczema medications for the 6-week study treatment period.
  • Subjects must not be enrolled in another investigational drug study.
  • Subjects must not be allergic to silver or cocoa butter.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double
Enrollment
180 participants

Interventions

  • DrugNanocrystalline silver cream (NPI)
06

Study locations

19 sites
  • Radiant Research
    Birmingham, Alabama 35209, United States
  • Medical Affliated Research Centers, Inc.
    Huntsville, Alabama 35801, United States
  • National Jewish Medical & Research Center
    Denver, Colorado 80206, United States
  • nTouch Research
    Washington, District of Columbia 20037, United States
  • Radiant Research
    West Palm Beach, Florida 33407, United States
  • Radiant Research
    Boise, Idaho 83704, United States
  • Radiant Research
    Overland Park, Kansas 66215, United States
  • Radiant Research
    St. Louis, Missouri 63141, United States
  • Sadick Dermatology & Aesthetic Surgery
    New York, New York 10021, United States
  • Mount Sinai School of Medicine
    New York, New York 10029, United States
  • Clinical Research of Winston-Salem, Inc.
    Winston Salem, North Carolina 27103, United States
  • University Hospitals of Cleveland
    Cleveland, Ohio 44106, United States
  • Radiant Research
    Columbus, Ohio 43212, United States
  • Oregon Health & Science University
    Portland, Oregon 97239, United States
  • Radiant Research
    Philadelphia, Pennsylvania 19115, United States
  • National Allergy, Asthma & Urticaria Centers of Charleston, P.A.
    Charleston, South Carolina 29407, United States
  • Radiant Research
    Greer, South Carolina 29605, United States
  • ACE Research Specialists, Inc.
    Nashville, Tennessee 37203, United States
  • Radiant Research
    Lakewood, Washington 98499, United States
07

References and documents

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2005, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00076375
Lead sponsor
Nucryst Pharmaceuticals
First posted
Jan 23, 2004
Start date
Nov 2003
Completion
Apr 2004
Last update
Jun 24, 2005
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2004. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion