The Effect of Oral Administration of 9-cis β Carotene Rich Powder of the Alga Dunaliella Bardawil on Visual Functions in Adolescent Patients With Retinitis Pigmentosa
| Registry | NCT02018692 |
|---|---|
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Study type | Interventional; randomized, crossover, masking: quadruple, treatment |
| Enrollment | 30 (Estimated) |
| Sponsor | Sheba Medical Center (Other gov) |
| Conditions | Retinitis Pigmentosa |
| Interventions | Alga Dunaliella Bardawil powder, Placebo:Starch (Dietary supplement) |
| Dates | start 2026-03-01 (estimated), primary completion 2028-12-31 (estimated), completion 2028-12-31 (estimated), first posted 2013-12-23, last updated 2025-10-06 |
| Locations | 1 site in Israel |
Related Papers Related Patents Related Grants Related Experts
All trials for Retinitis Pigmentosa All trials of Alga Dunaliella Bardawil powder All trials of Placebo:Starch
The aim of this study is to determine whether 9-cis-beta Caroten rich D. Brdawiil extract is effective in the treatment of retinitis pigmentosa in adolescent patients.
Retinitis pigmentosa is a genetically disease consisting of progressive retinal degeneration starting in the rods. Its prevalence is 1:4000 people and is the fourth most common blinding disease in Israel in 2004 \[7% of all blindness\]. The investigators treated a non-progressive form of the disease \[Fundus Albipunctatus\] by oral therapy of the food supplement made from alga Dunaliella Bardawil composed of approximately 50% 9-cis β-carotene.
The 9-cis β -carotene has been shown to be a precursor of 9-cis retinoic acid both in-vitro in human intestinal mucosa and in-vivo in a ferret, perfused with 9-cis b-carotene. The night vision, as measured objectively by electroretinography (ERG) more than doubled in six patients tested following treatment. The visual field was also improved significantly. In a more recent study the investigators treated 29 retinitis pigmentosa patients with the 9-cis b Carotene algae Dunaliella Bardawil in a double masked placebo control cross over trial. Significant improvement in retinal function was recorded in 34% of the patients.
As a natural extension of this study we will perform a double-masked, randomized, crossover, placebo-controlled study for adolescent patients. Longer treatment duration will be tested: a 24 week treatment with either the 9-cis β-carotene-rich capsules or placebo followed by an additional a 24 week treatment with the other capsules and a wash-out period of 24 weeks between this two type of treatments. We predict that with this study design a maximal/increased therapeutic effect as well as efficient washout will be achieved.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Alga Dunaliella Bardawil 9-cis beta Carotene Rich Powder | Experimental | Dietary Supplement: Alga Dunaliella Bardawil powder; Dietary Supplement: Placebo:Starch | 15 patients will first receive the capsules containing the alga Dunaliella Bardawil 9-cis beta-Carotene rich powder (5mg/Kg) for 24 weeks. After 24 weeks of washout period they will receive capsule containing placebo (Starch) for 24 weeks. |
| Placebo (Starch) | Placebo comparator | Dietary Supplement: Alga Dunaliella Bardawil powder; Dietary Supplement: Placebo:Starch | The other 15 Patients will receive first the placebo (Starch) capsules for 24 weeks. After 24 weeks of washout period they will receive capsules containing the alga Dunaliella Bardawil 9-cis beta-Carotene rich powder . |
Sex: All, ages: 12 Years to 18 Years
Inclusion Criteria: * Written informed consent to participate in the study. * Adolescent 12-18 years old. * Electroretinogram (ERG) responses compatible with the diagnosis of Retinitis Pigmentosa Exclusion Criteria: * Currently a smoker * Current use of vitamin A/ β-carotene supplements * Active arterial disease within 3 months prior to enrolment in the study, e.g. unstable angina, myocardial infarction, transient ischemic attack, stroke, coronary artery bypass graft surgery * History of malignancy, excepting basal or squamous cell skin carcinoma * Females who are pregnant, or breast feeding, or are premenopausal but not using chemical or mechanical contraception * Uncontrolled hypertension, defined either as resting diastolic blood pressure >95 mmHg (taken from the mean of 3 readings) or as resting systolic blood pressure >180 mmHg * History of alcohol abuse or drug abuse or both * Intention to engage in vigorous exercise or an aggressive diet regimen * Uncontrolled endocrine or metabolic disease * Participation in another investigational drug study within 4 weeks prior to enrolment * Serious or unstable medical or psychological condition which, in the opinion of the PI, would compromise the subject's safety or successful participation in the study * Initiation of hormone replacement therapy or oral contraceptive therapy within 3 months prior to enrolment
| Facility | City | Country | Status |
|---|---|---|---|
| Goldschleger Eye Research Institute, Sheba Medical Center, | Tel Litwinsky | Israel |