NCT05707442RecruitingPhase 3
Stent Implantation Versus Medical Therapy for Idiopathic IntracraniaL Hypertension (SIMPLE)
Source: ClinicalTrials.gov · Last updated 10 Feb 2026
Brief summary (registry, in English)
The aim of this study is to assess the efficacy of stent implantation versus medical therapy on idiopathic intracranial hypertension with venous sinus stenosis.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 74 (estimated)
- First submitted
- 25 Dec 2022
- Start date
- 16 Feb 2023
- Primary completion date
- Jan 2027
- Lead sponsor
- Beijing Tiantan Hospital
- Diseases
- High blood pressure
- NCT number
- NCT05707442
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 74
- From 16 Feb 2023 to the primary completion date, Jan 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Ophthalmic Exclusion Criteria:
- Current intraocular pressure \> 28mmHg or previous intraocular pressure \> 30mmHg
- Refractive error spherical power greater than -6.0D or +6.0D and astigmatism greater than 3.0D, except for the following cases:
- Myopia of - 6.0D to - 8.0D with the following: 1)There was no myopia related disease that can lead to decreased vision under the eyeground microscope (eg, scleral staphyloma, retinal thinning at the posterior pole, and moderate to severe disc tilt); 2) The patient wore contact lenses of appropriate degree for all visual field examinations.
- Hyperopia of +6.0D to +8.0D with the following: 1) The presence of a well characterized peri optic disc edematous halo, as opposed to crowded small optic discs or other features of decreased visual acuity associated with hyperopic changes, was at the discretion of the site investigator or reading center leader (or his designee); 2) The patient wore contact lenses of appropriate degree for all visual field examinations.
- Examination visible or past medical history known to have large optic disc drusen (persistent optic disc edema can present with small optic disc drusen, as low numbers are acceptable for inclusion and to be determined by the investigator to be unrelated to vision loss)
Lab values
- Subject Exclusion Criteria
- Previous surgery for IIH, including optic nerve sheath fenestration (ONSF), CSF shunting, decompressive craniectomy or venous sinus stenting
- Progressive or rapid visual loss needed urgent surgical intervention; if delay\>24-48 h consider interim lumbar drain (for rapid visual loss only).Surgical options to consider: CSF diversion or optic nerve sheath fenestration
- Visual loss due to other etiologies (eg, retinal drusen, retinal and optic neuropathy, cataracts, etc)
- Other condition requiring the use of diuretics, steroids or other drugs to reduce intracranial pressure
- DSA showed diffused venous sinus stenosis, cortical or deep vein stenosis
- A history of severe thyroid disease and iodine allergy
- Pregnant or lactating women
- Severe cardiopulmonary, liver or kidney failure
- Known hereditary or acquired haemorrhagic diathesis
- Known hereditary or acquired thrombophilia
- Platelet counts or coagulation abnormality
- Major surgery or severe trauma or any traumatic brain injury within the previous 14 days
- A history of cerebral hemorrhage, arteriovenous malformation, intracranial aneurysm or tumor
- Other life threatening illness (eg, advanced cancer) likely to lead to death within a few months; the physical, psychological and social status of patients may affect follow-up (eg, drug addiction, advanced malignant disease, no telephone, no family, etc); cannot tolerate general anesthesia
- Increased intracranial pressure due to other secondary factors
Who the study is looking for
- Subject Eligibility Criteria
- Diagnosis of IIH by modified Dandy criteria about for more than 2 months
- Lumbar puncture opening pressure ≥250 mmH₂O within 6 weeks before enrollment
- Normal cerebrospinal fluid (CSF) composition
- Neuroimaging showing normal brain parenchyma without hydrocephalus, mass, or any structural lesion and no evidence of meningeal enhancement on CT or MRI
- Localized venous sinus stenosis (VSS) with stenotic degree ≥ 50% on DSA, and pressure gradient across stenosis ≥ 8 mmHg
- Patients or their relatives signed written informed consent
- Ophthalmic Eligibility Criteria:
- At least one eye had the presence of papilledema
- At least one eye of visual field loss: PMD ranging from - 2dB and below; decreased visual function on automated perimetry was reproducible with a false-positive rate of no more than 15%
- Visual acuity above 20 / 200 (≥ 39 letters)
Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Beijing Tiantan Hospital Coordinator of this site? Confirm its status | Beijing | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.