Clinical Trials Directory

Trials / Terminated

TerminatedNCT00369499

STOP PAIN: Septal Closure of PFO - Does it Prevent Migraine?

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
656 (estimated)
Sponsor
Abbott Medical Devices · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this Study is to compare the effect of transcatheter device closure of atrial shunting to a non-closure control group over a period from cessation of procedure related medication at 3 months until 9 months post randomization by determining the proportion of patients that experience a 50% or more reduction in the baseline monthly migraine attack frequency in each group.

Conditions

Interventions

TypeNameDescription
DEVICEPFO Closure

Timeline

Start date
2007-03-01
Completion
2009-06-01
First posted
2006-08-29
Last updated
2023-06-29

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00369499. Inclusion in this directory is not an endorsement.