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NCT01651559

A Double Blind Controlled Clinical Trial Comparing The Efficacy Of A Dead Sea Mineral Enriched Body Cream vs Its Carrier as an Adjuvant Treatment For Psoriatic Patients Undergoing Phototherapy

Status unknown Last updated 14 November 2012
What this trial tests

trial in Psoriasis Vulgaris in 50 participants. Status unknown.

Timeline
1 November 2012
Primary endpoint
1 June 2013
1 June 2013

Quick facts

Lead sponsorAhava Dead Sea Laboratories
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment50
Start date1 November 2012
Primary completion1 June 2013
Estimated completion1 June 2013
Sites2 locations across Israel

Conditions studied

Sponsor

Ahava Dead Sea Laboratories

Who can join

Adults 18 to 70, any sex, with Psoriasis Vulgaris. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This is a two-center study aimed to assess the efficacy of Dead Sea Minerals in alleviating symptoms of Psoriasis Vulgaris, in 50 patients undergoing phototherapy. A bilateral left right comparison will be made, after using the study product and the placebo, for 8 weeks, twice daily, on each of the body sides (left right). In addition to the clinical evaluations, skin biochemistry will be studied using non-invasive techniques. The latter will be correlated with the clinical results of the patients. These will serve for future development of diagnostic assays and personalized therapies.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Psoriasis Vulgaris

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01651559.

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