← Eichor
Study identifier: NCT06759428 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Registry of Chronic Subdural Hematoma

Condition: Chronic Subdural Hematoma · Registry  ·  Sponsor: Erasmus Medical Center

PhaseN/A
Planned participants1500
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this observational study is to better understand how chronic subdural hematoma (CSDH) progresses and how patients are treated and cared for. The study focuses on three main questions: 1. What are the characteristics of patients with CSDH when they are diagnosed? 2. What treatments do patients with CSDH receive? 3. What are the outcomes for patients with CSDH, including their functional ability, cognitive health, and neurological status? Participants will receive their usual standard treatment. As part of the study, they will complete a brief telephone interview three months after their treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Rahman Fakhry  ·  +31 10 7043507  ·  r.fakhry@erasmusmc.nl

Dana C. Holl  ·  d.holl@erasmusmc.nl

Always discuss trial participation with your own doctor first.

Locations (2)

Amsterdam UMCAmsterdam, NetherlandsRecruiting
Erasmus MCRotterdam, NetherlandsRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06759428