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Clinical Trial Summary

Idiopathic intracranial hypertension (IIH) is a condition of unknown etiology, primarily affecting overweight females of childbearing age. Typically, patients experience headache and visual symptoms due to increased intracranial pressure (ICP) and papilledema. The diagnosis is difficult, and outcomes vary from no sequelae to blindness or chronic headaches. No clear prognostic indicators exist. Treatment consists of medication, weight loss, and possibly surgical intervention.There is an unmet need of defining biomarkers with prognostic or diagnostic value and defining predictors of a poor outcome. This project is a prospective, population-based cohort study including clinical data and a biobank (blood samples and cerebrospinal fluid). The investigator's primary aim is to identify biomarkers of diagnostic or prognostic value and to create a clinical IIH database. The clinical database will answer questions about patient characteristics at baseline and during follow-up, identify predictors of outcome, and help create a standardized programme for follow-up and


Clinical Trial Description

This study is a multicenter, prospective, population-based cohort study with consecutive inclusion of patients in which the diagnosis of IIH is suspected. This study is carried out in collaboration between the Danish Headache Center, Rigshospitalet-Glostrup, and the Neurological Department at Odense University Hospital. Patients are eligible for inclusion into the study if: 1. IIH is suspected 2. > 18 years old and able to provide written informed consent. At baseline included patients will have: A.) Medical history B.) Neurological, ophthalmological and general medical examination C.) Relevant neuro-imaging D.) Blood samples and lumbar puncture F.) Evaluation by other specialist, including neuro-psychologists, if appropriate. Subsequently patients are divided into three sub-groups according to revised Friedmann criteria: 1. Certain IIH or IIH-WOP 2. Suspected, but unconfirmed, IIH 3. IIH ruled out Patients are followed at a headache center and by neuro-ophthalmologist according to standard clinical practice. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04032379
Study type Observational [Patient Registry]
Source Danish Headache Center
Contact Johanne Severinsen, M.D.
Phone 004538633553
Email johanne.juhl.severinsen@regionh.dk
Status Recruiting
Phase
Start date February 14, 2018
Completion date May 31, 2027

See also
  Status Clinical Trial Phase
Terminated NCT02541994 - Axial Length and Central Corneal Thickness in Benign Intracranial Hypertension N/A