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Clinical Trial Summary

A remotely administered study, non-randomized, non-blinded, controlled parallel assignment phase 2 trial to determine if oral inosine or inositol hexaphosphate will provide an effective long-term therapy to combat or slow neural damage progression either concurrently with existing iron chelation therapy or during the natural course of the disorder. Clinical changes in hearing, balance, and mobility, and cognition will be assessed for 36 months through patient-reported outcomes of study assigned assessments.


Clinical Trial Description

Capsules containing over-the-counter dietary supplement formulas of inosine 500 mg or 500 mg of inositol hexaphosphate(IP6) will be taken orally, two capsules two times per day for 36 months. Initial screening will determine patient arm assignment. Before dosing begins, patients will submit copies of previous audiogram results (3yrs), radiology reports (3yrs), and MRI series (3yrs) if available and complete baseline assessment activities: Montreal Cognitive Assessment (MoCA) administered remotely, Timed Up, and Go (TUG), 2-Minute Walk Test (2-MWT), The Activities-specific Balance Confidence (ABC) Scale, iSS-QoL (custom) patient outcome reported Assessment will take place four times: baseline, end-of-year 1 (12mo), end-of-year 2 (24mo), end-of-study (36mo). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04890808
Study type Interventional
Source Superficial Siderosis Research Alliance Inc.
Contact Rori-Suzanne Daniel
Phone 9035594123
Email administrator@superficialsiderosis.org
Status Not yet recruiting
Phase N/A
Start date May 2023
Completion date September 2027

See also
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Completed NCT01284127 - Observational Study of Deferiprone (Ferriprox®) in the Treatment of Superficial Siderosis