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Atrial FibrillationNigAfibRegNCT05936164

Nigeria Atrial Fibrillation Registry

An observational study of Atrial Fibrillation, run by University College Hospital, Ibadan.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

Atrial fibrillation is the most common sustained cardiac arrhythmia (rhythm abnormality) encountered in clinical practice. It contributes significantly to the risk of cardiac symptoms, hospital admissions, cardiovascular related morbidity and mortality and increased healthcare cost. Read more about this study

Who is it for?
Ages 15 to 100 years
Conditions the study is for
Atrial Fibrillation
How many people
4,000 participants
Where
No sites listed yet
Study dates
1 Oct 2023to 31 Dec 2028
How long will I take part?
1 Year
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 100 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Subjects are eligible to participate if they are 15 years and above and have 12-lead ECG features of atrial fibrillation

Who may be able to join

  • All cases of confirmed atrial fibrillation

Who cannot join

  • Refusal of consent

About this study

Official title: The Nigeria National Registry of Atrial Fibrillation

Atrial fibrillation is the most common sustained cardiac arrhythmia (rhythm abnormality) encountered in clinical practice. It contributes significantly to the risk of cardiac symptoms, hospital admissions, cardiovascular related morbidity and mortality and increased healthcare cost.

AF has significant impact on healthcare cost. The major drivers of the cost are hospitalisations, stroke and loss of productivity. Globally AF accounts for less than 1% of all deaths. However, because it co-exists with other conditions, it contributes to worse prognosis compared to persons who do not have AF. New onset AF in HF patients may be associated with particularly poor prognosis.

Read more

Most of the published data and current knowledge on AF epidemiology are based on studies in Europe and North America. The information obtainable from previous studies in sub-Saharan Africa is limited. Many of the studies were retrospective. There is also paucity of information on burden of AF (both in hospital and community), clinical profile and outcome of AF in Nigeria in particular and Africa in general.

The primary objective of this study is to determine the clinical characteristics, outcome as well as cost genetic features of AF in Nigeria.

The project will provide information on: i. Hospital and community burden of AF in Nigeria; ii. Clinical features, mode of presentation and risk factors for AF; iii. Provide data on AF related outcomes as well as prognostic factors.

Read the detailed description

Background to the Research Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia (rhythm abnormality) encountered in clinical practice. (1) It contributes significantly to the risk of cardiac symptoms, hospital admissions, cardiovascular related morbidity and mortality and increased healthcare cost. (1, 2) In 2010, the Global Burden of Disease (GBD) study estimated that about 33.5 million people have AF globally which represents about 0.5% of the world population. (2) The increasing rate of AF has been attributed to the ageing of the world population, rise in the burden of cardiovascular risk factors such as overweight/obesity, high blood pressure, diabetes mellitus etc. (1, 2) In 2010, the Global Burden of Disease (GBD) study estimated that about 33.5 million people have AF globally. Between 1990 and 2010, the total number of deaths associated with AF in sub-Saharan Africa (SSA) increased from 441 to 1227 (196% change) The age standardized death rate (per 100,00) associated with AF rose from 0.4 to 0.6 (50% change) between 1990 and 2013. (1) Nigeria contributes to a large proportion of AF in SSA and little attention has been paid to this huge health problem.

Statement of the Problem AF has been shown to be associated with increased morbidity (especially increased association with the risk of development of heart failure (HF) and stroke, in addition to increased risk of mortality. AF is also a significant public health problem based on the fact that it accounts for about 1% of the National Health Service budget in many countries. In the United States of America (USA), the management of AF consumes about 16-26 billion dollars annually. The recent global burden of disease report has provided evidence of progressive increases in the overall burden, incidence, prevalence as well as AF associated mortality in ten-year period (1990-2010) in Africa and Nigeria contributes to a large proportion of this. Aging of the population is associated with vascular disease due to hypertension, atherosclerosis and other CVD risk factors which increase arterial stiffness, cause diastolic dysfunction and atrial volume overload resulting in AF. Most of the published data and current knowledge on AF epidemiology are based on studies in Europe and North America. The information obtainable from previous studies in sub-Saharan Africa is limited. Many of the studies were retrospective. There is also paucity of information on burden of AF (both in hospital and community), clinical profile and outcome of AF in Nigeria in particular and Africa in general.

Objectives of the Research Primary Objective The primary objective of this study is to determine the clinical characteristics, outcome as well as cost genetic features of AF in Nigeria.

Secondary Objectives-

  1. To determine the hospital prevalence, clinical features and modes of presentation of AF in Nigeria.
  2. To conduct and determine the community prevalence of AF in Nigeria
  3. To determine the risk factors of AF in Nigeria.
  4. To determine the complications of AF in Nigeria
  5. To ascertain the mode of management of AF in Nigeria.
  6. To determine the 12-months outcome of the condition and develop predictive models of outcome for AF in the country.

Research Questions

  1. What are the hospital and community prevalence of AF in Nigeria.
  2. What are the clinical features and modes of presentation of AF in Nigeria?
  3. What are the risk factors of AF in Nigeria?
  4. What are the complications of AF in Nigeria?
  5. What are the modes of management of AF in Nigeria?
  6. What are the 12-months outcomes of AF in the country and are there predictive models of outcome in the country? Brief Literature Review Globally it is estimated that there 2.7 million new cases in males and 2.0 million cases in females of AF. (1) The age adjusted mortality rate 1.6 and 1.7 for men and women respectively of AF has been reported. In terms of disability adjusted life years (DALYs), this is estimated as 64.5 and 45.9 per 100,000 populations for men and women respectively. (1) AF is associated with increased risk of mortality after adjusting for other confounders. In the Framingham Heart Study, AF was associated with 1.5-1.9-fold increase in mortality in over 40-years of follow-up. In the Olmsted County Study, the mortality associated with AF at 4- and 12- months was 17 and 23% respectively. Elderly individuals (aged 70 years and above in rural Tanzania have 1-year mortality of 50% and 66.6% in men and women respectively AF has significant impact on healthcare cost. The major drivers of the cost are hospitalisations, stroke and loss of productivity (3) Globally AF accounts for less than 1% of all deaths. However, because it co-exist with other conditions, it contributes to worse prognosis compared to persons who do not have AF. New onset AF in HF patients may be associated with particularly poor prognosis. (3) There is limited data on population/ hospital prevalence and incidence of AF in SSA in general and Nigeria (Africa's most populous nation in particular) The very few hospitals based data are from Cameroon, Ivory Coast, Kenya, Senegal and South Africa. Most were retrospective report. The few from Nigeria recruited very few subjects (less than 100) (4) In South Africa about 4.6% of patients seen in a cardiac clinic had AF giving a prevalence of 5.6/100,000 population per year. (16) The estimated prevalence in Ivory Coast is 5.5/100,000 population based on a retrospective review over a 10-year period. AF prevalence in Senegal was estimated as 5.4% and it accounted for 66% of all heart rhythm disorders in the country. About 162 patients out of 22,144 medical patients were reported to have AF /Flutter in a private tertiary hospital in Kenya giving a prevalence of 0.7%.

In a community-based study in Tanzania, the crude prevalence of AF was low (0.7%). This is lower than similar study in Europe and North America where the prevalence is about 10% (in those aged 80 years and above) and 5% in those aged 65 years and above respectively.

The prevalence of AF among Africa Americans is strikingly lower compared to their Caucasian counterpart even when the risk factors for AF are higher in the former.

Research Methodology Design The study shall be prospective, observational and shall be conducted in 6 hospitals in the six geopolitical regions of the country. The community survey shall be cross-sectional in randomly selected urban and rural areas in the six geopolitical regions in the country Study population Subjects are eligible to participate if they are 18 years and above and have 12-lead ECG features of AF.

Exclusion criteria Subjects who refuse to participate in the study and pregnant women. Consent Written and/or informed consent shall be obtained from the subjects prior to enrolment into the study.

Enrollment and data collection All subjects with clinical diagnosis of AF shall be recruited. Data from each subject shall be obtained using a uniform and standardized case report forms and a detailed clinical documentation on newly diagnosed/ newly presenting cases/ pre-existing cases of HF shall be carried out. The following data shall be obtained: study identification number, centre code, demographic data, date of diagnosis of HF and pre-admission history (previous heart failure related admissions). Others include NYHA functional class, symptoms, signs, self-reported cardiovascular risk factors, aetiological risk factors/ co-morbidities, blood investigations, 12-lead ECG, echocardiography, medications and 12-month outcome.

Follow up Follow-up of subjects shall be through clinic visits or via telephone (if patient can't come to the clinic). Telephone numbers of next of kin of patients shall also be obtained. The follow up period shall be at one month, six month and 12 months from the time of consent. This will be conducted through the use of research nurses. Information that shall be obtained during the follow-up period includes well-being of the patient, symptoms, signs, medications as well as outcome.

Data analysis Data shall be entered by experienced personnel on personal computers and analyzed with SPSS version 11.0 (SPSS, Inc. Chicago Illinois) Other statistical packages such as STATA and SAS shall be used where necessary. Descriptive statistics for baseline data will be performed on continuous variables using mean, standard deviation, range and median where appropriate. Categorical variables shall be expressed as percentages. McNemar and chi-square tests (for categorical variables) and Student's t-test or analysis of variance (for continuous variables) shall be used for comparisons as appropriate. Advanced statistical analysis e.g. regression analysis shall be applied as necessary.

Data dissemination plan Publication policy will be decided by a writing committee consisting of all the members of the steering committee and the principal investigators from all participating sites. However, all the members of the steering committee, all principal investigators and all those considered by the steering committee to have contributed sufficiently to the study will be co-authors of the primary publications.

Expected Results The project will provide information on: i. Burden of AF in Nigeria; ii. Clinical features, mode of presentation and risk factors for AF; iii. Provide data on AF related outcomes as well as prognostic factors.

Keywords
Atrial fibrillation, arrhythmias, heart failure
Medical subject headings
Atrial Fibrillation, Arrhythmias, Cardiac, Heart Failure

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. All cause mortality

    All deaths

    Measured: 12 months

Secondary outcomes (3)
  1. Hospitalisation

    All hospital readmissions

    Measured: At 12 months

  2. Stroke

    All forms of stroke

    Measured: 12 months

  3. Any other thromboembolic events

    Any other thromboembolic events

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Jul 2023
  2. Study start1 Oct 2023 (estimated)
  3. Primary completion1 Oct 2027 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
4,000 participants (estimated)
Target duration
1 Year
IDs, dates and publications
ClinicalTrials.gov ID
NCT05936164
Sponsor's protocol ID
NigAfibRegistry_V.2
Acronym
NigAfibReg
Status last verified
Jun 2023
First submitted
29 Jun 2023
Last updated
7 Jul 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Atrial Fibrillation, run by University College Hospital, Ibadan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 7 Jul 2023. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

All cause mortality (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Jul 2023.

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