Outcomes Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF)

Sponsor
Janssen Scientific Affairs, LLC (Industry)
Overall Status
Completed
CT.gov ID
NCT01165710
Collaborator
Duke Clinical Research Institute (Other), Bayer (Industry)
10,179
171
54
59.5
1.1

Study Details

Study Description

Brief Summary

The ORBIT-AF registry will be a multicenter, prospective outpatient disease registry to identify "real world" treatment patterns of atrial fibrillation. The registry will describe this patient population with regards to demographics, clinical factors, risk stratification, and geographic regions. In particular, attention will be focused on the utilization, effectiveness, and safety of antithrombotic therapies in the prevention of stroke. The registry is designed to identify reasons and risk factors for non-receipt of anticoagulation (AC) therapy, as well as reasons why AF patients who are prescribed AC therapy do not take them.

Condition or Disease Intervention/Treatment Phase
  • Other: Patients with Atrial Fibrillation (AF)

Detailed Description

The ORBIT-AF registry is a multicenter prospective outpatient disease registry of patients with incident (initial diagnosis) or prevalent (existing diagnosis) atrial fibrillation (AF) that will analyze treatment patterns and outcomes in patients with AF in the US. Approximately 10,000 prospective cohort of patients will be enrolled. The registry will be a nation-wide collaboration of Health Care Providers (e.g., cardiologists, internists, primary care physicians, electrophysiologists, quality improvement personnel, office/practice managers, research coordinators, and pharmacists). This collaborative effort will be focused on the optimization of outpatient management of patients with AF. Consecutive patients who meet the eligibility criteria will be approached and educated about the registry. Patients who express interest will provide informed consent. Patients enrolled in the registry will be followed for approximately 3 years. Patient follow-up by their AF care provider will continue as scheduled according to local clinical practice. Patient Reported outcome (PRO) questionnaires will be administered to a sub-sample of approximately 1,500 patients. For patients who consent to answer PRO questionnaires, these questionnaires will be administered by the site to the patient at the baseline visit [except the baseline Anticoagulation-Related Treatment Satisfaction (ACTS)] and during their regularly scheduled follow-up visits. The baseline ACTS for incident patients will be completed and returned back to the site at least 4 weeks after starting antithrombotic therapies. The ACTS questionnaire will only be administered to patients who are taking antithrombotic therapies within the 4 weeks before a visit or newly prescribed antithrombotic therapies. Data collection will occur at 6-month intervals for a minimum of 3 years (baseline, 6 months, 12 months, 18 months, 24 months, 30 months, and 36 months). The data collection windows will be wide (3 months in either direction) in order to maximize data collection during the patients regularly scheduled follow-up with their AF care provider. Collection of Patient Reported Outcome (PRO) Questionnaires will not continue beyond the 24-month data collection interval. Atrial Fibrillation Data capture will include demographics, cardiovascular risk factors, diagnosis, type of AF (paroxysmal, persistent, permanent AF), treatment strategy (rate vs. rhythm), ablation history, cardioversions, antithrombotic therapy decisions and monitoring (INRs), concomitant medications and doses, insurance and provider information, AF quality-of-life, anticoagulation treatment satisfaction, caregiver assistance, pet ownership, comorbidities, compliance, and outcomes. Pre-defined outcomes of interest will include stroke or non-CNS (non-systemic) embolism, major adverse cardiac events, all-cause mortality, cause-specific death (sudden, non-sudden, heart failure-related), major bleeding, AF-related quality of life, anticoagulation-related treatment satisfaction, all-cause hospitalization and specific anticoagulation outcomes (e.g. time in therapeutic range and primary discontinuation of oral anticoagulation). The data generated by this registry will be used to identify real world practice, especially as it compares and relates to guidelines set forth by the American College of Cardiology, American Heart Association and European Society of Cardiology for the management of patients with AF. Observational Study - No investigational drug administered. For any patients receiving the sponsor's drug, Xarelto (rivaroxaban), under the direction of a physician, all serious adverse events and all non-serious related events will be reported to the sponsor (Janssen Scientific Affairs, LLC)

Study Design

Study Type:
Observational
Actual Enrollment :
10179 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Outcomes Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF)
Study Start Date :
Jun 1, 2010
Actual Primary Completion Date :
Nov 1, 2014
Actual Study Completion Date :
Dec 1, 2014

Arms and Interventions

Arm Intervention/Treatment
001

Patients with Atrial Fibrillation (AF) Treatment patterns of AF according to patient demographics clinical factors risk stratification and geographic regions.

Other: Patients with Atrial Fibrillation (AF)
Treatment patterns of AF according to patient demographics, clinical factors, risk stratification, and geographic regions.

Outcome Measures

Primary Outcome Measures

  1. The primary outcome is stroke or non-CNS (systemic) embolism. Key primary objective is: characterize & describe the AF patient population as a whole, with emphasis on demographics, comorbidities, and risk profiles. [3 years]

Secondary Outcome Measures

  1. The number of major adverse cardiac events. [3 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult patients with incident (initial diagnosis) or prevalent (existing diagnosis) AF with electrocardiographic documentation

  • anticipated ability to adhere to local regularly scheduled follow-up visits

Exclusion Criteria:
  • Anticipated life expectancy less than 6 months

  • short lasting AF secondary to a reversible condition (e.g. hyperthyroidism, pulmonary embolism, post-cardiothoracic surgery)

  • Participation in a randomized trial of anticoagulation for AF at the time of enrollment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Birmingham Alabama United States
2 Dothan Alabama United States
3 Huntsville Alabama United States
4 Mobile Alabama United States
5 Montgomery Alabama United States
6 Pell City Alabama United States
7 Tuscaloosa Alabama United States
8 Cottonwood Arizona United States
9 Tucson Arizona United States
10 Fort Smith Arkansas United States
11 Carlsbad California United States
12 Carmichael California United States
13 Corona California United States
14 Laguna Hills California United States
15 Long Beach California United States
16 Los Alamitos California United States
17 Los Angeles California United States
18 Montebello California United States
19 Northridge California United States
20 Orange California United States
21 Oxnard California United States
22 Palo Alto California United States
23 Pismo Beach California United States
24 Pomona California United States
25 San Diego California United States
26 San Ramon California United States
27 Santa Rosa California United States
28 Tarzana California United States
29 Torrance California United States
30 Tustin California United States
31 Ventura California United States
32 Aurora Colorado United States
33 Colorado Springs Colorado United States
34 Golden Colorado United States
35 Newark Delaware United States
36 Seaford Delaware United States
37 Boynton Beach Florida United States
38 Coral Springs Florida United States
39 Deerfield Beach Florida United States
40 Fort Myers Florida United States
41 Fort Walton Beach Florida United States
42 Hollywood Florida United States
43 Jupiter Florida United States
44 Lakeland Florida United States
45 Oakland Park Florida United States
46 Orange Park Florida United States
47 Ormond Beach Florida United States
48 Port Charlotte Florida United States
49 St. Petersburg Florida United States
50 Tallahassee Florida United States
51 Atlanta Georgia United States
52 Decatur Georgia United States
53 Marietta Georgia United States
54 Riverdale Georgia United States
55 Idaho Falls Idaho United States
56 Nampa Idaho United States
57 Aurora Illinois United States
58 Evergreen Park Illinois United States
59 Melrose Park Illinois United States
60 Peoria Illinois United States
61 Rock Island Illinois United States
62 Rockford Illinois United States
63 Urbana Illinois United States
64 Winfield Illinois United States
65 Bloomington Indiana United States
66 Evansville Indiana United States
67 Hammond Indiana United States
68 Indianapolis Indiana United States
69 La Porte Indiana United States
70 South Bend Indiana United States
71 Waterloo Iowa United States
72 Overland Park Kansas United States
73 Crestview Hills Kentucky United States
74 Lexington Kentucky United States
75 Owensboro Kentucky United States
76 Alexandria Louisiana United States
77 Rockport Maine United States
78 Beltsville Maryland United States
79 Salisbury Maryland United States
80 Biddeford Massachusetts United States
81 Bay City Michigan United States
82 Bridgman Michigan United States
83 Commerce Township Michigan United States
84 Grand Blanc Michigan United States
85 Lansing Michigan United States
86 Livonia Michigan United States
87 Mount Clemens Michigan United States
88 Stevensville Michigan United States
89 Traverse City Michigan United States
90 Troy Michigan United States
91 Minneapolis Minnesota United States
92 Anaconda Montana United States
93 Omaha Nebraska United States
94 Las Vegas Nevada United States
95 Bridgewater New Jersey United States
96 Elmer New Jersey United States
97 Haddon Heights New Jersey United States
98 Linden New Jersey United States
99 Nampa New Jersey United States
100 Ridgewood New Jersey United States
101 Sewell New Jersey United States
102 Toms River New Jersey United States
103 Flushing New York United States
104 Huntington New York United States
105 Jamaica New York United States
106 New York New York United States
107 Northport New York United States
108 Calabash North Carolina United States
109 Charlotte North Carolina United States
110 Durham North Carolina United States
111 Greenwood North Carolina United States
112 Jacksonville North Carolina United States
113 Pinehurst North Carolina United States
114 Raleigh North Carolina United States
115 Sanford North Carolina United States
116 Tabor City North Carolina United States
117 Winston Salem North Carolina United States
118 Fargo North Dakota United States
119 Minot North Dakota United States
120 Mansfield Ohio United States
121 Miamisburg Ohio United States
122 Piqua Ohio United States
123 Toledo Ohio United States
124 Worthington Ohio United States
125 Youngstown Ohio United States
126 Abington Pennsylvania United States
127 Beaver Pennsylvania United States
128 Danville Pennsylvania United States
129 Doylestown Pennsylvania United States
130 Erie Pennsylvania United States
131 Lansdale Pennsylvania United States
132 Philadelphia Pennsylvania United States
133 Scranton Pennsylvania United States
134 Spring House Pennsylvania United States
135 West Reading Pennsylvania United States
136 Wynnewood Pennsylvania United States
137 Yardley Pennsylvania United States
138 Pawtucket Rhode Island United States
139 Anderson South Carolina United States
140 Easley South Carolina United States
141 Spartanburg South Carolina United States
142 Harriman Tennessee United States
143 Kingsport Tennessee United States
144 Nashville Tennessee United States
145 Arlington Texas United States
146 Beaumont Texas United States
147 Corpus Christi Texas United States
148 Flower Mound Texas United States
149 Fort Worth Texas United States
150 Houston Texas United States
151 Mcallen Texas United States
152 Odessa Texas United States
153 Plano Texas United States
154 San Antonio Texas United States
155 Tomball Texas United States
156 Salt Lake City Utah United States
157 Fredericksburg Virginia United States
158 Lynchburg Virginia United States
159 Midlothian Virginia United States
160 Roanoke Virginia United States
161 Winchester Virginia United States
162 Burien Washington United States
163 Port Orchard Washington United States
164 Spokane Washington United States
165 Tacoma Washington United States
166 Vancouver Washington United States
167 La Crosse Wisconsin United States
168 Madison Wisconsin United States
169 Hato Rey Puerto Rico
170 Rio Grande Puerto Rico
171 San Juan Puerto Rico

Sponsors and Collaborators

  • Janssen Scientific Affairs, LLC
  • Duke Clinical Research Institute
  • Bayer

Investigators

  • Study Director: Janssen Scientific Affairs, LLC Clinical Trial, Janssen Scientific Affairs, LLC

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Janssen Scientific Affairs, LLC
ClinicalTrials.gov Identifier:
NCT01165710
Other Study ID Numbers:
  • CR016327
  • RIVAROXAFL4001
First Posted:
Jul 20, 2010
Last Update Posted:
Jan 24, 2017
Last Verified:
Jan 1, 2017
Keywords provided by Janssen Scientific Affairs, LLC
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 24, 2017