Toggle Main Menu Toggle Search

Open Access padlockePrints

Cerebrospinal fluid shunting or dural venous sinus stenting to preserve vision in idiopathic intracranial hypertension (IIH Intervention): protocol for an open-label, multicentre, randomised controlled phase IIb trial

Lookup NU author(s): Professor Phil WhiteORCiD

Downloads


Licence

This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

© Author(s) (or their employer(s)) 2026. Re-use permitted under CC BY. Published by BMJ Group. INTRODUCTION: Idiopathic intracranial hypertension (IIH) is characterised by raised intracranial pressure (ICP) and typically affects young women with obesity. Patients are at risk of permanent visual loss due to papilloedema. Some require emergency intervention to rapidly reduce papilloedema and preserve vision. The international standard of care for patients with sight-threatening IIH is cerebrospinal fluid (CSF) shunting. However, dural venous sinus stenting (DVSS) is an emerging procedure that is offered at many neuroscience centres internationally as the primary intervention. Currently, there are no randomised controlled trial data supporting the efficacy of any interventional approach for preserving vision in sight-threatening IIH. METHODS AND ANALYSIS: IIH Intervention is a UK-based two-arm, open-label, multicentre, randomised controlled phase IIb clinical trial with integrated health economic evaluation to compare CSF shunting with DVSS in patients who have confirmed IIH and are at risk of permanent visual loss due to severe papilloedema. The primary outcome is the global thickness of the peripapillary retinal nerve fibre layer (RNFL), an indicator of papilloedema, measured by optical coherence tomography (OCT) over a 6-month period. Secondary outcomes are global thickness of the RNFL over 12 and 24 months, as well as macular ganglion cell layer volume, perimetric mean deviation, headache outcomes, intervention reporting measures (including complications and revisions) and patient-reported outcomes over 6, 12 and 24 months. ETHICS AND DISSEMINATION: The protocol was approved initially on 12 December 2022 by West Midlands-South Birmingham Research Ethics Committee (ref: 22/WM/0230). Participants will be required to provide written informed consent. The results of this trial will be disseminated through national and international presentations and peer-reviewed publications. TRIAL REGISTRATION NUMBER: ISRCTN57142415.


Publication metadata

Author(s): Tsermoulas G, Mollan SP, Homer V, Kristunas C, White P, Wakerley BR, Toma AK, Robertson F, Berman G, Ahmed F, Atan D, Bandyopadhyay S, Barton D, Booth T, Bremner F, Denton A, Downer J, Edwards R, Frew E, Gew JJY, Hill LJ, Hughes T, Lax S, Macdonald J, Maxwell G, McHugh J, Shah P, Taleti E, Tasker R, Thomas S, Joannides AJ, Sinclair A

Publication type: Article

Publication status: Published

Journal: BMJ Open

Year: 2026

Volume: 16

Issue: 8

Online publication date: 03/08/2026

Acceptance date: 15/07/2026

Date deposited: 17/08/2026

ISSN (print): 2044-6055

ISSN (electronic): 2044-6055

Publisher: BMJ Publishing Group

URL: https://doi.org/10.1136/bmjopen-2025-111013

DOI: 10.1136/bmjopen-2025-111013

PubMed id: 42547236


Altmetrics

Altmetrics provided by Altmetric


Funding

Funder referenceFunder name
National Institute for Health Research (NIHR) Health Technology Assessment programme (NIHR131211)
Sir Jules Thorn Award for Biomedical Research

Share