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NCT01897545 · ClinicalTrials.gov registry record · Phase 2
Combined Treatment of Arterial Hypertension and Atrial Fibrillation
A Phase 2 study of Atrial Fibrillation and Arterial Hypertension, sponsored by Meshalkin Research Institute of Pathology of Circulation.
- Completed
- Registry status
- Phase 2
- Development phase
- 60
- Enrollment target
- 3
- Study locations
NCT01897545 is a Phase 2 study of Atrial Fibrillation and Arterial Hypertension that has completed, run by Meshalkin Research Institute of Pathology of Circulation. The registered enrollment target is 60 participants, below the 2,997-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (98% lower). The trial reports 3 study locations across 2 states.
The verdict
NCT01897545, a Phase 2 study of Atrial Fibrillation and Arterial Hypertension, has completed, sponsored by Meshalkin Research Institute of Pathology of Circulation.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 60 participants
- Enrollment target
- 3
- Study locations
Study Summary
The purpose of this study is the comparative evaluation of systolic blood pressure (SBP) lowering, atrial fibrillation (AF) recurrence and clinical data in patients with paroxysmal/persistent AF and resistant/non-resistant hypertension, undergoing AF ablation alone or combined with percutaneous renal denervation.
Conditions Studied
Interventions
- PROCEDURE Circumferential PV isolation
- PROCEDURE PV isolation+renal denervation
Study Locations (3)
Other
- Athens Euroclinic - Athens
- State Research Institute of Circulation Pathology - Novosibirsk
New York
- The Valley Health System - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2012-04 |
| Est. Completion | 2013-06 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01897545
The ClinicalTrials.gov registry entry for NCT01897545 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,997-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (98% lower). The listed sponsor is Meshalkin Research Institute of Pathology of Circulation, which has 5 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Atrial Fibrillation appearing as the primary indexed condition, and to 2 interventions - of which Circumferential PV isolation is the first listed.
NCT01897545 reports 3 study locations spanning 2 distinct geographic areas - top geographies include Other, New York.
Frequently Asked Questions
What is clinical trial NCT01897545 about?
NCT01897545 is a clinical study titled "Combined Treatment of Arterial Hypertension and Atrial Fibrillation". The purpose of this study is the comparative evaluation of systolic blood pressure (SBP) lowering, atrial fibrillation (AF) recurrence and clinical data in patients with paroxysmal/persistent AF and resistant/non-resistant hypertension, undergoing AF ablation alone or combined with percutaneous rena...
What is the current status of trial NCT01897545?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2012-04. Estimated completion is 2013-06.
What conditions does trial NCT01897545 study?
This clinical trial studies the following conditions: Atrial Fibrillation, Arterial Hypertension.
What interventions are being tested in trial NCT01897545?
The interventions under investigation include: Circumferential PV isolation (PROCEDURE), PV isolation+renal denervation (PROCEDURE).
Who is sponsoring clinical trial NCT01897545?
This trial is sponsored by Meshalkin Research Institute of Pathology of Circulation, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01897545 being conducted?
This trial has 3 study locations across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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