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Published on: October 17, 2017
The idiopathic intracranial hypertension treatment trial: clinical profile at baseline
Michael Wall1, Mark J Kupersmith2, Karl D Kieburtz3
1Department of Neurology, University of Iowa, Iowa City2Department of Ophthalmology, University of Iowa, Iowa City.
Insights
Idiopathic intracranial hypertension (IIH) predominantly affects obese young women. This study characterized IIH patients, revealing common symptoms like headache and visual field defects requiring formal perimetry for diagnosis.
Area of Science:
- Neurology
- Ophthalmology
- Clinical Research
Background:
- Idiopathic intracranial hypertension (IIH) lacks large prospective cohort data for disease characterization.
- The Idiopathic Intracranial Hypertension Treatment Trial (IIHTT) was established to address this knowledge gap.
Purpose of the Study:
- To report the baseline clinical and laboratory features of patients enrolled in the IIHTT.
- To characterize the disease in a large cohort of untreated IIH patients.
Main Methods:
- 165 patients meeting modified Dandy criteria for IIH were enrolled across 38 North American sites.
- Data collected via questionnaires, examinations, automated perimetry, and fundus photography.
- Inclusion criteria included perimetric mean deviation between -2 dB and -7 dB; most participants were women.
Main Results:
- The cohort comprised predominantly young, obese women (mean age 29.0 years, BMI 39.9).
- Common symptoms included headache (84%), transient visual obscurations (68%), and pulse synchronous tinnitus (52%).
- Visual field defects, primarily arcuate loss and enlarged blind spots, were prevalent, though visual acuity was often preserved.
Conclusions:
- IIH is primarily a disease of obese young women.
- Patients with mild visual loss present with characteristic symptoms and specific visual field defects.
- Formal perimetry is essential for detecting subtle visual field abnormalities in IIH.
Importance:
To our knowledge, there are no large prospective cohorts of untreated patients with idiopathic intracranial hypertension (IIH) to characterize the disease.
Objective:
To report the baseline clinical and laboratory features of patients enrolled in the Idiopathic Intracranial Hypertension Treatment Trial.
Design, Setting, And Participants:
We collected data at baseline from questionnaires, examinations, automated perimetry, and fundus photography grading. Patients (n = 165) were enrolled from March 17, 2010, to November 27, 2012, at 38 academic and private practice sites in North America. All participants met the modified Dandy criteria for IIH and had a perimetric mean deviation between -2 dB and -7 dB. All but 4 participants were women.
Main Outcomes And Measures:
Baseline and laboratory characteristics.
Results:
The mean (SD) age of our patients was 29.0 (7.4) years and 4 (2.4%) were men. The average (SD) body mass index (calculated as weight in kilograms divided by height in meters squared) was 39.9 (8.3). Headache was the most common symptom (84%). Transient visual obscurations occurred in 68% of patients, back pain in 53%, and pulse synchronous tinnitus in 52%. Only 32% reported visual loss. The average (SD) perimetric mean deviation in the worst eye was -3.5 (1.1) dB, (range, -2.0 to -6.4 dB) and in the best eye was -2.3 (1.1) dB (range, -5.2 to 0.8 dB). A partial arcuate visual field defect with an enlarged blind spot was the most common perimetric finding. Visual acuity was 85 letters or better (20/20) in 71% of the worst eyes and 77% of the best eyes. Quality of life measures, including the National Eye Institute Visual Function Questionnaire-25 and the Short Form-36 physical and mental health summary scales, were lower compared with population norms.
Conclusions And Relevance:
The Idiopathic Intracranial Hypertension Treatment Trial represents the largest prospectively analyzed cohort of untreated patients with IIH. Our data show that IIH is almost exclusively a disease of obese young women. Patients with IIH with mild visual loss have typical symptoms, may have mild acuity loss, and have visual field defects, with predominantly arcuate loss and enlarged blind spots that require formal perimetry for detection.
Trial Registration:
clinicaltrials.gov Identifier: NCT01003639.
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