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TRUfill®'s Line in Intracranial aNeurysm Embolisation (TRULINE)

C

Codman & Shurtleff

Status

Completed

Conditions

Aneurysms

Study type

Observational

Funder types

Industry

Identifiers

NCT01503775
NV-PMK-0902

Details and patient eligibility

About

The objective of this study is to evaluate the long term efficacy and safety of the CODMAN TRUFILL®'s line of coils in the treatment of patients with intracranial ruptured or non-ruptured aneurysms in real-life routine clinical practice.

Enrollment

171 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient ≥ 18 years old
  • Patient presenting one or more ruptured or non-ruptured intracranial aneurysms assessed by angiography
  • Patient implanted with one or more CODMAN TRUFILL® coils
  • Patient agree to take part in the study, or agreement of a representative of the patient in case of patient inability, after being informed by the investigator and have received information letter.

Exclusion criteria

  • Patient who does not accept to take part in the study after being informed
  • Patient already enrolled in a clinical trial involving experimental medication or device.

Trial design

171 participants in 1 patient group

TRUFILL® DCS Orbit Galaxy

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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