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Tinnitus clinical trials

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NCT ID: NCT01412918 Terminated - Tinnitus Clinical Trials

Inhibitor Masking Device & Sodium Channel, Voltage Gated, Type IX Alpha Subunit (SCN9) Gene Expression

Start date: September 2011
Phase: N/A
Study type: Interventional

To evaluate the effectiveness of the Inhibitorâ„¢ Tinnitus Masking Device. To determine if there is a higher incident of expression of the sodium channel, voltage gated, type IX alpha subunit (SCN9) gene in those subjects with disturbing tinnitus than subjects that are not disturbed by tinnitus.

NCT ID: NCT01385540 Terminated - Tinnitus Clinical Trials

Exploration of Cortical Neural Network in Patients With Bothersome Tinnitus

Start date: July 2011
Phase: N/A
Study type: Observational

This will be an experimental task-based functional MRI pilot study involving the neuroimaging assessment of patients with severely bothersome tinnitus, defined by a global bothersome scale. The investigators plan to enroll a total of 12 participants (6 severely bothered tinnitus and 6 age-matched non-tinnitus controls) over the course of six months to undergo task-based imaging. Subjects in the tinnitus group may have previously participated in the CTRWU study (HRPO: 07-0689) conducted by Dr. Jay Piccirillo at Washington University and have given permission to be contacted for consideration in future studies. The selected paradigm will allow us to advance knowledge about the role of the attention, control, and other cortical networks in the development and maintenance of bothersome tinnitus.

NCT ID: NCT00957788 Terminated - Tinnitus Clinical Trials

Safety Study for NST-001 and the Neuroject Injection Set to Treat Tinnitus

Start date: January 2009
Phase: Phase 1
Study type: Interventional

This research study involves an experimental drug (NST_001) and a delivery system. The main purpose of this research study is to investigate the safety of NST-001, delivered directly to the inner ear for the treatment of tinnitus.

NCT ID: NCT00845975 Terminated - Tinnitus Clinical Trials

Study of Low Level Laser Therapy and Tinnitus Relief

Start date: August 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if low level laser light therapy might help to relieve tinnitus in adults.

NCT ID: NCT00827008 Terminated - Subjective Tinnitus Clinical Trials

Open-Label, Long-Term Treatment Study, to Assess the Long-Term Safety and Tolerability and Efficacy of Neramexane in Patients With Subjective Tinnitus

OLLTT
Start date: January 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the long-term safety and tolerability and efficacy of neramexane mesylate in the long-term treatment of subjective tinnitus after a completed double-blind randomized placebo controlled study

NCT ID: NCT00591019 Terminated - Tinnitus Clinical Trials

Use of Modafinil in the Treatment of Tinnitus

Start date: August 2006
Phase: Phase 1
Study type: Interventional

A study on the effects of the FDA approved drug Modafinil upon attention problems associated with tinnitus. This is considered to be a safe drug with few side effects. Each subject will be asked to participate in 3 sessions each lasting approximately 1 hour in which cognitive testing and recordings will be taken. The study involves each subject taking a 2- week supply of Modafinil and a 2- week supply of placebo. We hypothesize inattention related to thalamocortical dysrhythmia found in tinnitus can be reduced by Modafinil thus improving vigilance.

NCT ID: NCT00317850 Terminated - Tinnitus Clinical Trials

Gabapentin for the Treatment of Tinnitus

Start date: April 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The specific aim of the Gabapentin for the Relief of Idiopathic Subjective Tinnitus Trial is to assess the therapeutic benefit of Gabapentin (Neurontin®) for subjective idiopathic troublesome tinnitus. We employed a double-blind placebo-controlled randomized clinical trial design to assess the efficacy of Gabapentin. Adults, between the ages of 18 and 70 with idiopathic, subjective, troublesome, unilateral or bilateral, non-pulsatile tinnitus of 6 month's duration or greater and score of 38 or greater on the Tinnitus Handicap Inventory were enrolled.