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NCT00569023

Treatment of Congenital Stationary Night Blindness With an Alga Containing High Dose of Beta Carotene

Completed NA Last updated 26 June 2012
What this trial tests

NA trial testing alga Dunaliella bardawil in Night Blindness in 7 participants. Completed in 1 July 2010.

Timeline
1 July 2007
Primary endpoint
1 August 2009
1 July 2010

Quick facts

Lead sponsorSheba Medical Center
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment7
Start date1 July 2007
Primary completion1 August 2009
Estimated completion1 July 2010
Sites1 location across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Sheba Medical Center

Who can join

Adults 18 to 75, any sex, with Night Blindness. 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

To assess the effect of oral administration of the alga Dunaliella bardawil containing approximately 50% all-trans beta-carotene and 50% 9-cis beta-carotene isomers on visual functions patients with Congenital Stationary Night Blindness {Fundus albipunctatus).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Sheba Medical Center trials

Trials by the same sponsor.

Verify against primary sources

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/NCT00569023.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing