Acute Changes in Bioimpedance During Cardiac Resynchronization Therapy (Impel)
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| ClinicalTrials.gov Identifier: NCT03640000 |
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Recruitment Status : Unknown
Verified August 2018 by Hans Henrik Odland, Oslo University Hospital.
Recruitment status was: Recruiting
First Posted : August 21, 2018
Last Update Posted : August 21, 2018
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Heart Failure, Systolic | Diagnostic Test: Impedance measurements in Cardiac Resynchronization therapy | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 60 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Diagnostic |
| Official Title: | Acute Changes in Bioimpedance During Cardia Resynchronization Therapy |
| Study Start Date : | January 2015 |
| Estimated Primary Completion Date : | December 2020 |
| Estimated Study Completion Date : | December 2021 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Determination of impedance signals
This single arm study is designed to measure impedance signals from implanted leads in different positions in the heart. Signals obtained at different pre specified position are compared to each other to determine the robustness of the acquired measurements.
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Diagnostic Test: Impedance measurements in Cardiac Resynchronization therapy
Bioimpedance measurements |
- Optimization of Bioimpedance measurements [ Time Frame: 3 years ]Acquisition of absolute and imaginary bioimpedance signals from electrodes of known location within the heart at different input current frequencies. Pacing is performed from Three different electrodes during acquisition of bioimpedance acquisition forming Three different groups. Wavelets of the signals are analyzed within each Group and compared within the Group and between the Groups. Optimization is achived when a discrimination factor that is calculated is improved.
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| Ages Eligible for Study: | 18 Years to 90 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03640000
| Contact: Hans Henrik Odland, MD, PhD | 23070000 ext +47 | h.h.odland@medisin.uio.no |
| Norway | |
| Oslo University Hospital | Recruiting |
| Oslo, Norway, 0027 | |
| Contact: Hans Henrik Odland hodland@ous-hf.no | |
| Principal Investigator: | Hans Henrik Odland, MD, PhD | Oslo University Hospital |
| Responsible Party: | Hans Henrik Odland, principal Investigator, Oslo University Hospital |
| ClinicalTrials.gov Identifier: | NCT03640000 |
| Other Study ID Numbers: |
2014/1223 |
| First Posted: | August 21, 2018 Key Record Dates |
| Last Update Posted: | August 21, 2018 |
| Last Verified: | August 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
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Heart Failure, Systolic Heart Failure Heart Diseases Cardiovascular Diseases |

