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Subjective Tinnitus clinical trials

View clinical trials related to Subjective Tinnitus.

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NCT ID: NCT05265949 Completed - Obesity Clinical Trials

The Effects of Weight Loss on Tinnitus Symptoms

Start date: April 23, 2019
Phase: N/A
Study type: Interventional

Subjective tinnitus is the perception of irregular sound at different frequencies. Although the underlying cause of tinnitus is unclear, increased body weight is known to increase tinnitus symptoms. This study aimed to determine the effects of dietary and physical activity interventions on tinnitus symptoms. Sixty-three obese subjects with tinnitus aged 20 to 65 years were divided into diet + physical 8 activity (P.A.), diet, P.A., and control groups. Dietary and anthropometric records, Tinnitus Handicap 9Inventory (THI), Beck Depression Inventory (BDI), Short-Form Health Survey (SF-36), and Visual Analogue Scale (VAS) of all individuals were compared at the baseline and at the end of the study.

NCT ID: NCT04829214 Completed - Subjective Tinnitus Clinical Trials

OTO-313 in Subjects With Unilateral Subjective Tinnitus

Start date: March 22, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy of OTO-313 in subjects with unilateral tinnitus and to determine the safety and tolerability of OTO-313 in subjects with unilateral tinnitus.

NCT ID: NCT04696588 Completed - Subjective Tinnitus Clinical Trials

Neck Kinesiotherapy and Massage in Tinnitus Treatment

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

The primary aim of this study is to investigate the effectiveness of cervical spine kinesiotherapy and massage in tinnitus treatment. Furthermore, we investigate if there is a link between cervical spine range of motion and cervical muscles tension and tinnitus.

NCT ID: NCT03550430 Completed - Tinnitus Clinical Trials

Neurofeedback for Tinnitus - Does Frequency Specificity Matter?

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

This study will evaluate the efficacy of an alpha/delta ratio (ADR) neurofeedback training protocol on tinnitus distress. 1/3 of the participants in the study will undergo ADR neurofeedback training, 1/3 an active comparator, beta/theta ratio (BTR) neurofeedback training, whilst the final 1/3 of participants will fill in daily diaries of tinnitus complaints and symptoms for two weeks.

NCT ID: NCT01268449 Completed - Subjective Tinnitus Clinical Trials

Evaluation of Low Dose Laser in Treatment of Tinnitus

Start date: March 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine wether low dose laser is effective on idiopathic subjective tinnitus.

NCT ID: NCT01177137 Completed - Subjective Tinnitus Clinical Trials

Tinnitus Retraining Therapy Trial

TRTT
Start date: July 2011
Phase: Phase 3
Study type: Interventional

The primary purpose of the Tinnitus Retraining Therapy Trial (TRTT) is to assess the efficacy of tinnitus retraining therapy (TRT) as a treatment for severe debilitating tinnitus. TRT is a non-medical intervention that uses directive counseling (DC) and sound therapy (ST)to habituate the patient's associated negative emotional reactions to tinnitus, its perception, and ultimately, its impact on the patient's life.

NCT ID: NCT00955799 Completed - Subjective Tinnitus Clinical Trials

Efficacy, Safety, Tolerability of Neramexane in Patients With Subjective Tinnitus

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of neramexane mesylate in the treatment of subjective tinnitus in comparison to placebo.

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: NCT00772980 Completed - Subjective Tinnitus Clinical Trials

Efficacy, Safety and Tolerability of Neramexane in Comparison to Placebo in Patients With Subjective Tinnitus

Start date: November 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of neramexane mesylate in the treatment of subjective tinnitus in comparison to placebo.

NCT ID: NCT00739635 Completed - Subjective Tinnitus Clinical Trials

Efficacy, Safety and Tolerability of Neramexane in Patients With Subjective Tinnitus

EASE
Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of neramexane mesylate in the treatment of subjective tinnitus in comparison to placebo.