Heart FailureNCT05936957
The Ibadan Acute and Chronic Heart Failure Project
An observational study of Heart Failure, run by University College Hospital, Ibadan at 1 site in Nigeria.
Trial summary
Contemporary studies from South Africa and Nigeria have built on historical reports to demonstrate that the etiology and indeed case profile of acute HF (i.e. more women and younger individuals affected in the prime of their life) is different from high-income countries. Read more about this study
- Who is it for?
- Ages 18 to 100 years
- Conditions the study is for
- Heart Failure
- How many people
- 2,000 participants
- Where
- 1 siteNigeria
- Study dates
- 1 Jan 2015to 31 Dec 2030
- How long will I take part?
- 5 Years
- 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 18 to 100 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: All adults aged 18-100 years presenting with heart failure
Who may be able to join
- All cases of heart failure
Who cannot join
- No consent to participate
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Nigeria1 site, 1 recruiting
- Recruiting
University College Hospital Ibadan
Ibadan, Oyo State, 200212
Okechukwu Ogah, PhD, +2348067747121, osogah56156@gmail.com
About this study
Contemporary studies from South Africa and Nigeria have built on historical reports to demonstrate that the etiology and indeed case profile of acute HF (i.e. more women and younger individuals affected in the prime of their life) is different from high-income countries. As such, HF is now responsible for 7-10% of medical admissions in the region.
These are entirely based on studies on acute HF and few on chronic HF. The nexus between endemic infections such as tuberculosis (TB) and HIV/AIDS and other non-communicable or non-infectious risk factors and HF in Africa is scarcely documented.
Read more
This study will assess the long-term outcomes, risk factors, clinical phenotypes, and genomics of HF in Ibadan, Nigeria, estimate catastrophic healthcare cost associated with CHF and how it affects evidence-based care; understand cultural and social conceptions of HF in the city and by extension in Nigeria.
Data from each subject shall be obtained using a uniform and standardized case report forms (CRF). A detailed clinical documentation on cases of HF will be undertaken.
All variables will be summarized using appropriate descriptive statistics. Means and proportions will be estimated with two-tailed 95% confidence intervals. Specified patients' outcomes will also be summarized using proportions. Factors associated wit patient outcomes will be investigated using multivariable logistic regression models. Crude and adjusted Odds Ratio (OR) with 95% confidence intervals (CI) will be estimated.
The primary event outcome of the study will be mortality by cause. Secondary event outcomes will include non-fatal major events (both resulting in and not resulting in admission).
Read the detailed description
Background and Purpose Heart failure (HF) has emerged a major global public health problem.(1,2) HF affects over 64 million people worldwide. (3) It is a highly symptomatic syndrome that affects 2-3% of the population in high income countries especially in people above the age of 65 years. (4 5) Until recently, little was known about the emerging problem of non-communicable forms of HF supplementing traditional pathways to the syndrome in sub-Saharan Africa due to infections and infestations. Contemporary studies from South Africa (6) and Nigeria (7) have built on historical reports to demonstrate that the aetiology and indeed case profile of acute HF (i.e. more women and younger individuals affected in the prime of their life) is different from high-income countries. As such, HF is now responsible for 7-10% of medical admissions in the region. (7) These are entirely based on studies on acute HF. There are only few data on chronic HF in Africa. Furthermore, the nexus between endemic infections such as tuberculosis (TB) and HIV/AIDS and other non-communicable or non-infectious risk factors and HF in Africa is scarcely documented.
Gaps in knowledge on heart failure in sub-Saharan Africa
- Co-morbidities in HF patients, which are common and important to outcomes, have not been well studied in large cohorts in sub-Saharan Africa (SSA).
- The role and co-occurrence of infection such as tuberculosis and HIV /AIDS has not been extensively explored in the region.
4 There is paucity of information on the long-term outcome of HF in SSA (rehospitalization and mortality) 5 Current phenotypes of HF (HFrEF, HFpEF, HFmrEF), their clinical and sociodemographic predictors, management and outcomes are not well described in SSA.
6 There is also paucity of data on the assessment of barriers to HF care in SSA.
7 Significantly, given its potential enormous cost implications (both related to direct health care costs and economic burden on affected individuals and their families) there is virtually no data on the economic burden of HF in SSA.
8 There is paucity of data on cultural and social conceptions of heart failure in SSA.
9 There are few genetic and genomic HF studies in sub-Saharan Africa especially in Nigeria (the region's most populous country).
10 We do not know to what extent are standard care pathways and evidence-based treatment algorithms applied in the management of HF Ibadan. We also do not know to what extent high out of pocket expenses contribute to low levels of treatment. Furthermore, we do not know the scope for quality improvement to improve outcomes and reduce mortality rates in Nigeria.
11 Although there is existing evidence of economic cost and impact from the Abeokuta HF registry, data on catastrophic healthcare spending linked to CHF care from a household perspective are lacking. In addition, the extent to which out of pocket costs (drugs and consultations/ admissions) act as a barrier to continuing evidence-based care is not available.
12 Lastly the extent patient-centred approaches (their values and preference) are applied to care plans in Ibadan is not available. The use of patient-reported outcome measures in routine care (PROMs) has not been explored.
Aim The primary objective of this study is to assess the long-term outcomes, risk factors, clinical phenotypes, and genomics of HF in Ibadan, Nigeria, estimate catastrophic healthcare cost associated with CHF and how it affects evidence-based care; understand cultural and social conceptions of HF in the city and by extension in Nigeria Objectives
- To define the clinical profile of heart failure in Ibadan, Nigeria
- To determine the short-term, medium-term and long-term outcome of heart failure in Ibadan and by extension in Nigeria.
- To identify comorbidities (Infections and non-infections) in heart failure in Nigeria and the clinical implications
- To develop predictive models of mortality, rehospitalization and complications associated with heart failure in Nigeria.
- To estimate the catastrophic healthcare cost of HF in Ibadan
- To develop a community engagement and education programmes on non-communicable diseases (NCDs).
- To explore the cultural and social conceptions of heart failure in Ibadan, Nigeria.
- To investigate genetic associations of ACE, LMNA and Troponin T (TNNT2) variants with HF in the study population METHODS Study design The study shall be prospective study. It is expected that about 2500-3000 subjects with HF shall be recruited over a 5-year period and followed up at 6, 12, 24 months and five years.
Study location The study shall be conducted at the University College Hospital, Ibadan, Nigeria. The University College Hospital, Ibadan is the oldest teaching hospital in Nigeria and affiliated to the University of Ibadan. Currently the hospital has over 950 bed spaces and 163 examination couches and a current bed occupancy rate of 55-60%. The hospital has over 60-clinical departments. It serves a population of over 10million people and receives referrals from all over the country and as well from the West African sub-region.
Inclusion and exclusion criteria Subjects are eligible to participate if they are 18 years and older and have clinically and echocardiographically confirmed HF.
Data collection and case definition Data from each subject shall be obtained using a uniform and standardized case report forms (CRF). A detailed clinical documentation on cases of HF will be undertaken. The following data shall be obtained: study identification number, 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, aetiology of HF, co-morbidities, blood investigations, point of care biomarker, Chest X-ray, 12-lead ECG, echocardiography, medications, barriers to care, quality of life data etc.
Case definition The European Society of Cardiology guideline shall be employed for the diagnosis of HF. All cases shall be confirmed at echocardiography. All the echocardiograms shall be performed by trained personnel. The quality assurance information of the procedure at Ibadan has been published.
Blood Collection and Testing Blood sample will be obtained during the enrolment visit and shipped to the central laboratory at Ibadan for analysis of biochemical biomarkers, including risk factors for HF and related cardiovascular diseases.
Follow-up Follow-up of subjects shall be through clinic visits or via telephone. Telephone numbers of next of kin of patients shall also be obtained. Information that shall be obtained during the follow-up period shall include amongst others: well-being of the patient, symptoms, signs, medications as well as well as events such as readmission, deaths etc.
Deaths shall be recorded and their cause shall be ascertained by the review of various source documents or verbal autopsy to classify the cause of death.
Medication Adherence Questions regarding medication adherence will be asked at baseline and 1-year visit. This medication adherence questionnaire will ask questions on how often patients take their HF medicines, what factors/events may lead to their missing medicines, and reasons why they may miss medications.
Capture of dietary Questionnaire Dietary questionnaire shall be administered on the patients. This will be used to collect information about the type, portion size, quantity and frequency of commonly consumed foods. This will incorporate validated nutritional information in Nigeria.
Economic cost analysis Healthcare costs shall be estimate for one year in the Nigerian Naira and will be converted to US Dollar [$US] at the prevailing exchange rate at the time of the study. Catastrophic healthcare spending (CHS) occurs when out-of-pocket payments is above a given percentage of households' total income/total expenditure. Three thresholds, 10%, 20% and 40% will be applied to ascertain the burden of catastrophic healthcare spending among patients' household level.
Sample size calculation Though this study is prospective in design, it is largely exploratory because most of the objectives are descriptive in nature. For a descriptive study, a sample size of 400 is sufficient to estimate the level of any outcome with 95% confidence. However, to make adequate allowance for study objectives that requires comparisons, we plan to recruit at least of 1500-2000 patients.
Statistical analysis All variables will be summarised using appropriate descriptive statistics. Means and proportions will be estimated with two-tailed 95% confidence intervals. Specified patients' outcomes will also be summarised using proportions. Factors associated with patients' outcomes will be investigated using multivariable logistic regression models. Crude and adjusted Odds Ratio (OR) with 95% confidence intervals (CI) will be estimated Ethical considerations Ethical standard The Ibadan Acute and Chronic Heart Failure Project will be conducted in full compliance with the principles of the Declaration of Helsinki or with the laws and regulations of Nigeria.
Data management and statistical analysis Categorical variables shall be displayed as frequencies and proportions. Group comparison shall be done with the student's t-test and Chi square statistics shall be used for comparison of categorical variables. Survival function estimates shall be performed using the Kaplan-Meier method and the difference shall be tested using log-rank test. The follow up shall be censored at 6, 12 and 24 months.
- Conditions
- Heart Failure
- Keywords
- Heart failure, Cardiac Failure
- Medical subject headings
- Heart Failure
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Acute heart failure | These are acutely decompensated heart failure | |
| Chronic heart failure | These are stable heart failure patients being followed up in the outpatient clinic |
What is being measured
The primary outcome is the main question the study is designed to answer.
Mortality
All cause mortality
Measured: 5 years
Secondary outcomes (1)
Hospitalisation
Hospital readmission
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Jul 2023
- Study start1 Jan 2015
- Primary completion31 Dec 2025 (estimated)
- Study completion31 Dec 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (7)Papers the sponsor has linked to this study.
- Other trials for Heart FailureStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- 2,000 participants (estimated)
- Target duration
- 5 Years
Sponsor and investigators
- Lead sponsor
- University College Hospital, Ibadan
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, O.S Ogah, University College Hospital, Ibadan
- Investigators
- Okechukwu S Ogah, PhD, Principal investigator, Cardiology Unit, Department of Medicine, University College Hospital Ibadan, Nigeria
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05936957
- Sponsor's protocol ID
- IHFP_Protocol_V1.2_2015
- Other IDs
- 190371
- Status last verified
- Jun 2023
- First submitted
- 2 Sep 2022
- Last updated
- 10 Jul 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: There is no plan for this
Publications
Benjamin EJ, Blaha MJ, Chiuve SE, Cushman M, Das SR, Deo R, de Ferranti SD, Floyd J, Fornage M, Gillespie C, Isasi CR, Jimenez MC, Jordan LC, Judd SE, Lackland D, Lichtman JH, Lisabeth L, Liu S, Longenecker CT, Mackey RH, Matsushita K, Mozaffarian D, Mussolino ME, Nasir K, Neumar RW, Palaniappan L, Pandey DK, Thiagarajan RR, Reeves MJ, Ritchey M, Rodriguez CJ, Roth GA, Rosamond WD, Sasson C, Towfighi A, Tsao CW, Turner MB, Virani SS, Voeks JH, Willey JZ, Wilkins JT, Wu JH, Alger HM, Wong SS, Muntner P; American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association. Circulation. 2017 Mar 7;135(10):e146-e603. doi: 10.1161/CIR.0000000000000485. Epub 2017 Jan 25. No abstract available.
PubMed 28122885Cowie MR, Mosterd A, Wood DA, Deckers JW, Poole-Wilson PA, Sutton GC, Grobbee DE. The epidemiology of heart failure. Eur Heart J. 1997 Feb;18(2):208-25. doi: 10.1093/oxfordjournals.eurheartj.a015223. No abstract available.
PubMed 9043837Bui AL, Horwich TB, Fonarow GC. Epidemiology and risk profile of heart failure. Nat Rev Cardiol. 2011 Jan;8(1):30-41. doi: 10.1038/nrcardio.2010.165. Epub 2010 Nov 9.
PubMed 21060326Redfield MM, Jacobsen SJ, Burnett JC Jr, Mahoney DW, Bailey KR, Rodeheffer RJ. Burden of systolic and diastolic ventricular dysfunction in the community: appreciating the scope of the heart failure epidemic. JAMA. 2003 Jan 8;289(2):194-202. doi: 10.1001/jama.289.2.194.
PubMed 12517230Mosterd A, Hoes AW, de Bruyne MC, Deckers JW, Linker DT, Hofman A, Grobbee DE. Prevalence of heart failure and left ventricular dysfunction in the general population; The Rotterdam Study. Eur Heart J. 1999 Mar;20(6):447-55.
PubMed 10213348Damasceno A, Mayosi BM, Sani M, Ogah OS, Mondo C, Ojji D, Dzudie A, Kouam CK, Suliman A, Schrueder N, Yonga G, Ba SA, Maru F, Alemayehu B, Edwards C, Davison BA, Cotter G, Sliwa K. The causes, treatment, and outcome of acute heart failure in 1006 Africans from 9 countries. Arch Intern Med. 2012 Oct 8;172(18):1386-94. doi: 10.1001/archinternmed.2012.3310.
PubMed 22945249Ogah OS, Stewart S, Falase AO, Akinyemi JO, Adegbite GD, Alabi AA, Ajani AA, Adesina JO, Durodola A, Sliwa K. Contemporary profile of acute heart failure in Southern Nigeria: data from the Abeokuta Heart Failure Clinical Registry. JACC Heart Fail. 2014 Jun;2(3):250-9. doi: 10.1016/j.jchf.2013.12.005. Epub 2014 Apr 30.
PubMed 24952692
Study at a glance
From the registry record, last updated by the sponsor on 10 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Ibadan Acute and Chronic Heart Failure Project
- ClinicalTrials.gov ID
- NCT05936957
- Acronym / sponsor ID
- IHFP_Protocol_V1.2_2015
- Conditions
- Heart Failure
- Keywords
- Heart failure, Cardiac Failure
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 2,000 participants (estimated)
- Lead sponsor
- University College Hospital, IbadanUniversity, hospital or other
- Study start
- 1 Jan 2015 (actual)
- Primary completion
- 31 Dec 2025 (estimated)
- Study completion
- 31 Dec 2030 (estimated)
- First posted
- 10 Jul 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Contemporary studies from South Africa and Nigeria have built on historical reports to demonstrate that the etiology and indeed case profile of acute HF (i.e. more women and younger individuals affected in the prime of their life) is different from high-income countries. As such, HF is now responsible for 7-10% of medical admissions in the region.
These are entirely based on studies on acute HF and few on chronic HF. The nexus between endemic infections such as tuberculosis (TB) and HIV/AIDS and other non-communicable or non-infectious risk factors and HF in Africa is scarcely documented.
This study will assess the long-term outcomes, risk factors, clinical phenotypes, and genomics of HF in Ibadan, Nigeria, estimate catastrophic healthcare cost associated with CHF and how it affects evidence-based care; understand cultural and social conceptions of HF in the city and by extension in Nigeria.
Data from each subject shall be obtained using a uniform and standardized case report forms (CRF). A detailed clinical documentation on cases of HF will be undertaken.
All variables will be summarized using appropriate descriptive statistics. Means and proportions will be estimated with two-tailed 95% confidence intervals. Specified patients' outcomes will also be summarized using proportions. Factors associated wit patient outcomes will be investigated using multivariable logistic regression models. Crude and adjusted Odds Ratio (OR) with 95% confidence intervals (CI) will be estimated.
The primary event outcome of the study will be mortality by cause. Secondary event outcomes will include non-fatal major events (both resulting in and not resulting in admission).
Detailed description
Background and Purpose Heart failure (HF) has emerged a major global public health problem.(1,2) HF affects over 64 million people worldwide. (3) It is a highly symptomatic syndrome that affects 2-3% of the population in high income countries especially in people above the age of 65 years. (4 5) Until recently, little was known about the emerging problem of non-communicable forms of HF supplementing traditional pathways to the syndrome in sub-Saharan Africa due to infections and infestations. Contemporary studies from South Africa (6) and Nigeria (7) have built on historical reports to demonstrate that the aetiology and indeed case profile of acute HF (i.e. more women and younger individuals affected in the prime of their life) is different from high-income countries. As such, HF is now responsible for 7-10% of medical admissions in the region. (7) These are entirely based on studies on acute HF. There are only few data on chronic HF in Africa. Furthermore, the nexus between endemic infections such as tuberculosis (TB) and HIV/AIDS and other non-communicable or non-infectious risk factors and HF in Africa is scarcely documented.
Gaps in knowledge on heart failure in sub-Saharan Africa
- Co-morbidities in HF patients, which are common and important to outcomes, have not been well studied in large cohorts in sub-Saharan Africa (SSA).
- The role and co-occurrence of infection such as tuberculosis and HIV /AIDS has not been extensively explored in the region.
4 There is paucity of information on the long-term outcome of HF in SSA (rehospitalization and mortality) 5 Current phenotypes of HF (HFrEF, HFpEF, HFmrEF), their clinical and sociodemographic predictors, management and outcomes are not well described in SSA.
6 There is also paucity of data on the assessment of barriers to HF care in SSA.
7 Significantly, given its potential enormous cost implications (both related to direct health care costs and economic burden on affected individuals and their families) there is virtually no data on the economic burden of HF in SSA.
8 There is paucity of data on cultural and social conceptions of heart failure in SSA.
9 There are few genetic and genomic HF studies in sub-Saharan Africa especially in Nigeria (the region's most populous country).
10 We do not know to what extent are standard care pathways and evidence-based treatment algorithms applied in the management of HF Ibadan. We also do not know to what extent high out of pocket expenses contribute to low levels of treatment. Furthermore, we do not know the scope for quality improvement to improve outcomes and reduce mortality rates in Nigeria.
11 Although there is existing evidence of economic cost and impact from the Abeokuta HF registry, data on catastrophic healthcare spending linked to CHF care from a household perspective are lacking. In addition, the extent to which out of pocket costs (drugs and consultations/ admissions) act as a barrier to continuing evidence-based care is not available.
12 Lastly the extent patient-centred approaches (their values and preference) are applied to care plans in Ibadan is not available. The use of patient-reported outcome measures in routine care (PROMs) has not been explored.
Aim The primary objective of this study is to assess the long-term outcomes, risk factors, clinical phenotypes, and genomics of HF in Ibadan, Nigeria, estimate catastrophic healthcare cost associated with CHF and how it affects evidence-based care; understand cultural and social conceptions of HF in the city and by extension in Nigeria Objectives
- To define the clinical profile of heart failure in Ibadan, Nigeria
- To determine the short-term, medium-term and long-term outcome of heart failure in Ibadan and by extension in Nigeria.
- To identify comorbidities (Infections and non-infections) in heart failure in Nigeria and the clinical implications
- To develop predictive models of mortality, rehospitalization and complications associated with heart failure in Nigeria.
- To estimate the catastrophic healthcare cost of HF in Ibadan
- To develop a community engagement and education programmes on non-communicable diseases (NCDs).
- To explore the cultural and social conceptions of heart failure in Ibadan, Nigeria.
- To investigate genetic associations of ACE, LMNA and Troponin T (TNNT2) variants with HF in the study population METHODS Study design The study shall be prospective study. It is expected that about 2500-3000 subjects with HF shall be recruited over a 5-year period and followed up at 6, 12, 24 months and five years.
Study location The study shall be conducted at the University College Hospital, Ibadan, Nigeria. The University College Hospital, Ibadan is the oldest teaching hospital in Nigeria and affiliated to the University of Ibadan. Currently the hospital has over 950 bed spaces and 163 examination couches and a current bed occupancy rate of 55-60%. The hospital has over 60-clinical departments. It serves a population of over 10million people and receives referrals from all over the country and as well from the West African sub-region.
Inclusion and exclusion criteria Subjects are eligible to participate if they are 18 years and older and have clinically and echocardiographically confirmed HF.
Data collection and case definition Data from each subject shall be obtained using a uniform and standardized case report forms (CRF). A detailed clinical documentation on cases of HF will be undertaken. The following data shall be obtained: study identification number, 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, aetiology of HF, co-morbidities, blood investigations, point of care biomarker, Chest X-ray, 12-lead ECG, echocardiography, medications, barriers to care, quality of life data etc.
Case definition The European Society of Cardiology guideline shall be employed for the diagnosis of HF. All cases shall be confirmed at echocardiography. All the echocardiograms shall be performed by trained personnel. The quality assurance information of the procedure at Ibadan has been published.
Blood Collection and Testing Blood sample will be obtained during the enrolment visit and shipped to the central laboratory at Ibadan for analysis of biochemical biomarkers, including risk factors for HF and related cardiovascular diseases.
Follow-up Follow-up of subjects shall be through clinic visits or via telephone. Telephone numbers of next of kin of patients shall also be obtained. Information that shall be obtained during the follow-up period shall include amongst others: well-being of the patient, symptoms, signs, medications as well as well as events such as readmission, deaths etc.
Deaths shall be recorded and their cause shall be ascertained by the review of various source documents or verbal autopsy to classify the cause of death.
Medication Adherence Questions regarding medication adherence will be asked at baseline and 1-year visit. This medication adherence questionnaire will ask questions on how often patients take their HF medicines, what factors/events may lead to their missing medicines, and reasons why they may miss medications.
Capture of dietary Questionnaire Dietary questionnaire shall be administered on the patients. This will be used to collect information about the type, portion size, quantity and frequency of commonly consumed foods. This will incorporate validated nutritional information in Nigeria.
Economic cost analysis Healthcare costs shall be estimate for one year in the Nigerian Naira and will be converted to US Dollar [$US] at the prevailing exchange rate at the time of the study. Catastrophic healthcare spending (CHS) occurs when out-of-pocket payments is above a given percentage of households' total income/total expenditure. Three thresholds, 10%, 20% and 40% will be applied to ascertain the burden of catastrophic healthcare spending among patients' household level.
Sample size calculation Though this study is prospective in design, it is largely exploratory because most of the objectives are descriptive in nature. For a descriptive study, a sample size of 400 is sufficient to estimate the level of any outcome with 95% confidence. However, to make adequate allowance for study objectives that requires comparisons, we plan to recruit at least of 1500-2000 patients.
Statistical analysis All variables will be summarised using appropriate descriptive statistics. Means and proportions will be estimated with two-tailed 95% confidence intervals. Specified patients' outcomes will also be summarised using proportions. Factors associated with patients' outcomes will be investigated using multivariable logistic regression models. Crude and adjusted Odds Ratio (OR) with 95% confidence intervals (CI) will be estimated Ethical considerations Ethical standard The Ibadan Acute and Chronic Heart Failure Project will be conducted in full compliance with the principles of the Declaration of Helsinki or with the laws and regulations of Nigeria.
Data management and statistical analysis Categorical variables shall be displayed as frequencies and proportions. Group comparison shall be done with the student's t-test and Chi square statistics shall be used for comparison of categorical variables. Survival function estimates shall be performed using the Kaplan-Meier method and the difference shall be tested using log-rank test. The follow up shall be censored at 6, 12 and 24 months.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 5 Years
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Acute heart failure | – | –These are acutely decompensated heart failure |
| Chronic heart failure | – | –These are stable heart failure patients being followed up in the outpatient clinic |
Who may qualify
- Ages
- 18 to 100 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- All adults aged 18-100 years presenting with heart failure
Key inclusion criteria (1 listed)
- All cases of heart failure
Key exclusion criteria (1 listed)
- No consent to participate
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Mortality
Time frame: 5 years
All cause mortality
1 secondary outcome
Hospitalisation
Time frame: 5 years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jul 2023.
- Results publication: PubMed 28122885Benjamin EJ, Blaha MJ, Chiuve SE, Cushman M, Das SR, Deo R, de Ferranti SD, Floyd J, Fornage M, Gillespie C, Isasi CR, Jimenez MC, Jordan LC, Judd SE, Lackland D, Lichtman JH, Lisabeth L, Liu S, Longenecker CT, Mackey RH, Matsushita K, Mozaffarian D, Mussolino ME, Nasir K, Neumar RW, Palaniappan L, Pandey DK, Thiagarajan RR, Reeves MJ, Ritchey M, Rodriguez CJ, Roth GA, Rosamond WD, Sasson C, Towfighi A, Tsao CW, Turner MB, Virani SS, Voeks JH, Willey JZ, Wilkins JT, Wu JH, Alger HM, Wong SS, Muntner P; American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association. Circulation. 2017 Mar 7;135(10):e146-e603. doi: 10.1161/CIR.0000000000000485. Epub 2017 Jan 25. No abstract available.
- Results publication: PubMed 9043837Cowie MR, Mosterd A, Wood DA, Deckers JW, Poole-Wilson PA, Sutton GC, Grobbee DE. The epidemiology of heart failure. Eur Heart J. 1997 Feb;18(2):208-25. doi: 10.1093/oxfordjournals.eurheartj.a015223. No abstract available.
- Results publication: PubMed 21060326Bui AL, Horwich TB, Fonarow GC. Epidemiology and risk profile of heart failure. Nat Rev Cardiol. 2011 Jan;8(1):30-41. doi: 10.1038/nrcardio.2010.165. Epub 2010 Nov 9.
- Results publication: PubMed 12517230Redfield MM, Jacobsen SJ, Burnett JC Jr, Mahoney DW, Bailey KR, Rodeheffer RJ. Burden of systolic and diastolic ventricular dysfunction in the community: appreciating the scope of the heart failure epidemic. JAMA. 2003 Jan 8;289(2):194-202. doi: 10.1001/jama.289.2.194.
- Results publication: PubMed 10213348Mosterd A, Hoes AW, de Bruyne MC, Deckers JW, Linker DT, Hofman A, Grobbee DE. Prevalence of heart failure and left ventricular dysfunction in the general population; The Rotterdam Study. Eur Heart J. 1999 Mar;20(6):447-55.
- Results publication: PubMed 22945249Damasceno A, Mayosi BM, Sani M, Ogah OS, Mondo C, Ojji D, Dzudie A, Kouam CK, Suliman A, Schrueder N, Yonga G, Ba SA, Maru F, Alemayehu B, Edwards C, Davison BA, Cotter G, Sliwa K. The causes, treatment, and outcome of acute heart failure in 1006 Africans from 9 countries. Arch Intern Med. 2012 Oct 8;172(18):1386-94. doi: 10.1001/archinternmed.2012.3310.
- Results publication: PubMed 24952692Ogah OS, Stewart S, Falase AO, Akinyemi JO, Adegbite GD, Alabi AA, Ajani AA, Adesina JO, Durodola A, Sliwa K. Contemporary profile of acute heart failure in Southern Nigeria: data from the Abeokuta Heart Failure Clinical Registry. JACC Heart Fail. 2014 Jun;2(3):250-9. doi: 10.1016/j.jchf.2013.12.005. Epub 2014 Apr 30.
- Individual participant dataSharing planned: No. There is no plan for this
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Heart Failure
Recruiting
Achieving Optimal Medical Therapy Through Percutaneous Treatment of Secondary Mitral Regurgitation to Improve Outcome in Patients With HFrEF
Mitral Regurgitation Functional, Heart Failure With Reduced Ejection Fraction (HFrEF)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Okechukwu S Ogah, PhD principal investigator
Cardiology Unit, Department of Medicine, University College Hospital Ibadan, Nigeria
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Heart Failure, run by University College Hospital, Ibadan at 1 site in Nigeria.
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: looking for participants now, as of the sponsor's last update on 10 Jul 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Nigeria. Whether a site is taking part right now should be confirmed with that site. See every site.
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?
Contact Okechukwu S Ogah, PhD (+2348067747121, osogah56156@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Mortality (time frame: 5 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05936957, which also lists 7 linked publications.
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 10 Jul 2023.