Skip to main content
Clinical Trials/NL-OMON27414
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

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

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

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 Disease
NL-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 elderly
EUCTR2005-003821-25-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 Incontinence
EUCTR2005-000107-33-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 Incontinence
EUCTR2005-000107-33-SEaboratorios Dr. Esteve, S.A.180