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NCT06510582 · ClinicalTrials.gov registry record · Phase 1

Chronic Subdural Hematoma Treatment With Intra-Arterial Bevacizumab Injection

A Phase 1 study of Chronic Subdural Hematoma, sponsored by The Cooper Health System.

Recruiting
Registry status
Phase 1
Development phase
140
Enrollment target
1
Study location

NCT06510582: Recruiting Phase 1 study of Chronic Subdural Hematoma, sponsored by The Cooper Health System.

NCT06510582 is a Phase 1 study of Chronic Subdural Hematoma that is actively recruiting participants, run by The Cooper Health System. The registered enrollment target is 140 participants, below the 1,407-participant average among 4 other Chronic Subdural Hematoma trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06510582, a Phase 1 study of Chronic Subdural Hematoma, is actively recruiting participants, sponsored by The Cooper Health System.

RECRUITING
Registry status
Phase 1
Development phase
140 participants
Enrollment target
1
Study location

Study Summary

The goal of this clinical trial is to test whether infusing bevacizumab into the middle meningeal arteries can be used to treat chronic subdural hematomas (cSDH). The main questions it aims to answer are: * Is bevacizumab infusion safe in cSDH patients? * Is bevacizumab infusion effective in treating cSDH?

Primary Outcome

Reported serious adverse events classified using MedDRA and CTCAE, in addition to treatment-related events and all other adverse events

Conditions Studied

Interventions

  • DRUG Bevacizumab 2 mg/kg
  • DRUG Bevacizumab 4 mg/kg

Study Locations (1)

New Jersey

  • Cooper University Health Care - Camden

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2024-06-17
Est. Completion 2028-06
Phase Phase 1
The Cooper Health System

39 total trials

What NCT06510582 shows while recruiting

NCT06510582 is an interventional study that assigns participants to a tested intervention. The registered 140 participants enrollment target is mid-sized for trials with a published cap, below the 1,407-participant average among 4 other Chronic Subdural Hematoma trials with a reported enrollment target (90% lower).

The record links to 1 condition, with Chronic Subdural Hematoma appearing as the primary indexed condition, and to 2 interventions - of which Bevacizumab 2 mg/kg is the first listed.

NCT06510582 reports a single indexed study location in New Jersey.

Frequently Asked Questions

What is clinical trial NCT06510582 about?

NCT06510582 is a clinical study titled "Chronic Subdural Hematoma Treatment With Intra-Arterial Bevacizumab Injection". The goal of this clinical trial is to test whether infusing bevacizumab into the middle meningeal arteries can be used to treat chronic subdural hematomas (cSDH). The main questions it aims to answer are: * Is bevacizumab infusion safe in cSDH patients? * Is bevacizumab infusion effective in treat...

What is the current status of trial NCT06510582?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 140 participants. The study started on 2024-06-17. Estimated completion is 2028-06.

What conditions does trial NCT06510582 study?

This clinical trial studies the following conditions: Chronic Subdural Hematoma.

What interventions are being tested in trial NCT06510582?

The interventions under investigation include: Bevacizumab 2 mg/kg (DRUG), Bevacizumab 4 mg/kg (DRUG).

Who is sponsoring clinical trial NCT06510582?

This trial is sponsored by The Cooper Health System, which has 39 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06510582 being conducted?

This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06510582, the US trial registry maintained by the National Library of Medicine. NCT06510582 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.