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Sulodexide Efficacy in Chronic Idiopathic Subjective Tinnitus — SECIST  

Tinnitus, Subjective Clinical Trial

Official title:
Randomized Double Blind Controlled Trial on Sulodexide Efficacy in Chronic Idiopathic Subjective Tinnitus

Clinical Trial Summary

The objective of this prospective randomized and double blind controlled study is to evaluate the efficacy and safety of Sulodexide (25 mg) in the treatment of chronic idiopathic subjective tinnitus.

Clinical Trial Description

Patients with chronic idiopathic subjective tinnitus, since at least 1 year, re recruited from our Ear, Nose and Throat (ENT) clinic. After verification of inclusion and exclusion criteria, patients consenting to enter the study are assigned randomly to one of the following groups: 1- Sulodexide 25 mg for 40 days 2- Placebo for 40 days. Clinical evaluation of the patient is performed; tinnitus is assessed according to Tinnitus Handicap Inventory score, Mini Tinnitus Questionnaire score. Adverse effects are also noted. Patients are followed at 40 days post-treatment and outcome measures are assessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02737670
Study type Interventional
Source St Joseph University, Beirut, Lebanon
Contact
Status Completed
Phase Phase 2
Start date August 2014
Completion date August 2017
View Details
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