Nurse-assisted Intervention "eHealth@ Hospital -2-home"
NCT05750953
Cardiovascular Diseases, Colon Rectal Cancer
Stavanger, Rogaland, Norway
View Trial DetailsNCT Number: NCT00869921
Evaluate long-term performance of the 4195 LV Lead. This evaluation is based on the number of lead-related complications occuring during the study compared to the number of leads enrolled in the study. The leads will be followed for 5 years after implant. This study is required by FDA as a condition of approval of the Model 4195 LV Lead and is integrated within Medtronic's post-market surveillance platform.
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Observational
Calgary, Alberta, Canada
Model 4195 LV lead complication-free survivability will be summarized.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Patients who meet all of the following inclusion criteria and do not meet any of the following exclusion criteria are eligible for enrollment.
Inclusion criteria
Exclusion criteria
Time frame: Implant to 5 years post-implant.
Time frame: 5 years post implant
Medtronic
Industry
Attain StarFix® Model 4195 Left Ventricular Lead Chronic Performance Post Approval Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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