Cardiox Shunt Detection Technology Study
|ClinicalTrials.gov Identifier: NCT01333761|
Recruitment Status : Terminated (1)new FDS device design 2)improved Valsalva procedure 3)improved headbands and earpads.)
First Posted : April 12, 2011
Last Update Posted : January 9, 2013
Information provided by (Responsible Party):
Results Submitted - Not Posted on ClinicalTrials.gov
Results information has been submitted to ClinicalTrials.gov by the sponsor or investigator, but is not yet publicly available (or "posted") on ClinicalTrials.gov. The submitted information may not be available if it is pending Quality Control (QC) Review by the National Library of Medicine (NLM) or if issues identified during QC review are being addressed or corrected by the sponsor or investigator. NLM's limited QC review assesses for apparent errors, deficiencies, or inconsistencies. NLM staff do not verify the scientific validity or relevance of the submitted information.
|Recruitment Status :||Terminated|
|Actual Primary Completion Date :||July 2012|
|Actual Study Completion Date :||July 2012|
|Submission Cycle||Results Submitted to ClinicalTrials.gov||Results Returned after Quality Control Review|
|1||January 8, 2014|
|2||January 27, 2014||March 11, 2014|
Karttunen V, Ventilä M, Hillbom M, Salonen O, Haapaniemi H, Kaste M. Dye dilution and oximetry for detection of patent foramen ovale. Acta Neurol Scand. 1998 Apr;97(4):231-6.