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Not yet recruiting No phase listed Observational

Prospective Multi-center Single Arm Study for Subjects With Chronic Subdural Hematoma Treated With i-ED COILs, Either Alone or in Combination With Burr-holes or Mini-craniotomy

ClinicalTrials.gov ID: NCT07214623

Public ClinicalTrials.gov record NCT07214623. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 11:21 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

i-ED COIL Use for Reduction of Chronic Subdural Hematoma Post Market Study

Study identification

NCT ID
NCT07214623
Recruitment status
Not yet recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
Kaneka Medical America LLC
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

  • Neuro endovascular embolic coil Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 29, 2025
Primary completion
Nov 29, 2026
Completion
May 30, 2027
Last update posted
Oct 8, 2025

2025 – 2027

United States locations

U.S. sites
2
U.S. states
2
U.S. cities
2
Facility City State ZIP Site status
Westchester Medical Center Valhalla New York 10595
University of Pennslyvania Philadelphia Pennsylvania 11104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07214623, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 8, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07214623 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →