NL-OMON27414
Not yet recruiting
Not Applicable
A multicenter, double-blinded, randomised, 12 month, parallel group study to compare the efficacy of 48 mg BETahistine versus 8 [three times per day, tid] in the treatment of vertigo attacks in MENière's disease.
Prof. Dr. P.P.G. van Benthem (November 2015)Functie/ Position: Hoogleraar Keel-, neus-, oorheelkunde │Opleiding/Education: Studierichting/ Subject:T: +31 55 844 8207 │ F: +31 55 581 8194 │E: p.van.benthem@gelre.nl Prof. Dr. P.P.G. van Benthem (november 2015)University Medical Centre LeidenHead Otorhinolaryngolgy and Head- and Neck Surgery P.O. Box 96002300 RC Leiden0 sites74 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Menière's disease, betahistine, randomised controlled trial
- Sponsor
- Prof. Dr. P.P.G. van Benthem (November 2015)Functie/ Position: Hoogleraar Keel-, neus-, oorheelkunde │Opleiding/Education: Studierichting/ Subject:T: +31 55 844 8207 │ F: +31 55 581 8194 │E: p.van.benthem@gelre.nl Prof. Dr. P.P.G. van Benthem (november 2015)University Medical Centre LeidenHead Otorhinolaryngolgy and Head- and Neck Surgery P.O. Box 96002300 RC Leiden
- Enrollment
- 74
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
ot applicable
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Unilateral MD (definite or probable) according to diagnostic criteria derived from the American Academy Otolaryngology Head and Neck Surgery, Classification Committee of the Bárány Society, European Academy of Otology and Neurotology and International Classification of Vestibular Disorders published in 2015\.
- •2\. Age \> 18 years at the start of the trial.
Exclusion Criteria
- •1\.Bilateral MD.
- •2\.Severe disability (e.g. neurological, orthopedic, cardiovascular) or serious concurrent illness that might interfere with treatment or follow\-up.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Not yet recruiting
Not Applicable
FAIR-study.Chronic Obstructive Pulmonary DiseaseNL-OMON23638CROMSOURCE – Quality System Certified ISO 9001Lange Dreef 11H, NL-4131 NJ Vianen, The Netherlands144
Active, not recruiting
Phase 1
Trial to assess the effects of rimonabant 20 mg in patients with abdominal obesity and microalbuminuria, with type 2 diabetes mellitus or dyslipidaemia with or without other cardiometabolic risk factors.EUCTR2006-002951-33-ESsanofi-aventis, S.A.550
Active, not recruiting
Not Applicable
A 12 week multi-centre, randomized, double-blind, placebo controlled evaluation of the most efficacious and tolerable dose of escitalopram in the treatment of elderly patients. - Double-blind placebo controlled study of escitalopram in the treatment of depression in the elderlyDepression in the elderlyEUCTR2005-003821-25-DKPsychiatric Hospital189
Active, not recruiting
Phase 1
A 12-week multicentre, randomised, double-blind, parallel group, Phase IIpilot study to evaluate the efficacy and safety of cizolirtine citrate 200 mgbid (400 mg/d), cizolirtine citrate 300 mg bid (600 mg/d) and cizolirtinecitrate 400 mg bid (800 mg/d) versus placebo in the treatment of patientswith Stress Urinary Incontinence (SUI)Stress Urinary IncontinenceEUCTR2005-000107-33-ESaboratorios Dr. Esteve, S.A.180
Active, not recruiting
Not Applicable
A 12-week multicentre, randomised, double-blind, parallel group, Phase IIpilot study to evaluate the efficacy and safety of cizolirtine citrate 200 mgbid (400 mg/d), cizolirtine citrate 300 mg bid (600 mg/d) and cizolirtinecitrate 400 mg bid (800 mg/d) versus placebo in the treatment of patientswith Stress Urinary Incontinence (SUI)Stress Urinary IncontinenceEUCTR2005-000107-33-SEaboratorios Dr. Esteve, S.A.180