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Peripartum Cardiomyopathy in Nigeria Registry (PEACE)

Primary Purpose

Peripartum Cardiomyopathy

Status
Completed
Phase
Phase 4
Locations
Nigeria
Study Type
Interventional
Intervention
Oral Sodium Selenite 200 µg/day for 3 months
Sponsored by
Aminu Kano Teaching Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripartum Cardiomyopathy focused on measuring peripartum cardiomyopathy, Ventricular remodelling, Survival, Selenium, Oxidative stress, Nigeria

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Confirmed diagnosis of PPCM
  • PPCM patients with HF symptoms at the time of recruitment
  • Asymptomatic pregnant women attending antenatal clinic (ANC)
  • Sub-study: Open-label randomised Trial: Non-pregnant PPCM patients with all of the following: LVEF <35% and/or LVEDDi≤33.0 mm/m2 at 6 months postpartum AND selenium deficiency
  • Written informed consent

Exclusion Criteria:

  • Asymptomatic PPCM patients at the time of recruitment
  • PPCM patients who are not expected to survive at least 6 months from recruitment
  • Pregnant women with any medical condition other than PPCM
  • Subjects who are considered not likely to attend follow up reviews regularly, because of lack of patient's and close relative's phone numbers, or long distance from the study centre, etc
  • Refusal or withdrawal of consent

Sites / Locations

  • Aminu Kano Teaching Hospital
  • Aminu Kano Teaching Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Treatment

Control

Arm Description

Oral Sodium Selenite 200 µg/day for 3 months

No treatment

Outcomes

Primary Outcome Measures

Prevalence of peripartum cardiomyopathy (PPCM) in Nigeria
All participants confirmed to have PPCM presenting to the study centres, as described in PEACE Registry protocol V3.

Secondary Outcome Measures

Selenium deficiency in PPCM patients and apparently healthy pregnant women in Nigeria
Prevalence of selenium deficiency will be assessed. Serum selenium will be measured as described in PEACE Registry protocol V3. Selenium deficiency will be defined as serum selenium <70μg/L.
Oxidative stress in PPCM patients and apparently healthy pregnant women in Nigeria
Prevalence of oxidative stress will be assessed. Serum malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidise (GPO) and N-terminal pro-B-type natriuretic peptide (NT-BNP) will be measured as described in PEACE Registry protocol V3. Abnormal oxidative stress will be defined as the presence of serum NT-BNP >125pg/mL and ANY of the following: plasma MDA >1.25μmol/L, serum SOD >110ng/mL and plasma GPO >470U/L.
The effect of sodium selenite supplementation on cardiac function among PPCM patients.
PPCM patients with selenium deficiency, left ventricular ejection fraction (LVEF) <35% and/or insignificant left ventricular reverse remodeling (LVRR) at 6 months postpartum, will be offered sodium selenite 200mcg daily for 3 months, in an open-label randomized trial. LVRR would be defined as the presence of both absolute increase in LVEF ≥10.0% and decrease in LV end-diastolic dimension indexed to body surface area (LVEDDi) ≤33.0 mm/m2, while recovered LV systolic function as LVEF ≥55%, during the follow-up. Change in LVEF and LVEDDi will be measured at 6, 12, and 18 months follow up visits, to determine prevalence of LVRR among partipants on selenium treatment and those who will not be on selenium treatment.
Left Ventricular remodelling in PPCM patients
Change in LVEF and LVEDDi to determine LVRR
Right Ventricular (RV) remodelling in PPCM patients
Change in RV fractional area change (RVFAC) of the right ventricle (in cm2), to determine RV reverse remodelling (RVRR). RVRR is defined as RVFAC >35cm2.
Rehospitalisation rate
Number of participants who experience hospitalization for any cardiovascular disease during follow up.
Prevalence of cardio-embolic events
Number of participants who experience stroke, transient ischemic attack or any gangrene during the follow-up period of the study.
Survival rate
Number of participants who have survived the follow-up period of the study.

Full Information

First Posted
February 22, 2017
Last Updated
January 17, 2021
Sponsor
Aminu Kano Teaching Hospital
Collaborators
Nigerian Cardiac Society
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1. Study Identification

Unique Protocol Identification Number
NCT03081949
Brief Title
Peripartum Cardiomyopathy in Nigeria Registry
Acronym
PEACE
Official Title
Peripartum Cardiomyopathy in Nigeria (PEACE) A Registry to Study the Demographics, Social and Clinical Characteristics, Pathophysiology and Outcomes of Peripartum Cardiomyopathy in Nigeria
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
June 12, 2017 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aminu Kano Teaching Hospital
Collaborators
Nigerian Cardiac Society

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Peripartum cardiomyopathy (PPCM) is a global disease with significant morbidity and mortality, and Nigeria probably has the highest burden of the disease in the world. Unfortunately, much about the disease including its aetiology, epidemiology and treatment is not yet well described. This will be a prospective, national, multicenter cohort study, conducted in centres in Nigeria. It is expected that approximately 500 patients with PPCM and 500 apparently healthy pregnant women will be recruited over a 6-month period with follow-up at 3-monthly intervals for 18 months.
Detailed Description
Peripartum cardiomyopathy (PPCM) is a global disease with significant morbidity and mortality, and Nigeria probably has the highest burden of the disease in the world. Unfortunately, much about the disease including its aetiology, epidemiology and treatment is not yet well described. This will be a prospective, national, multicenter cohort study, conducted in centres in Nigeria. It is expected that approximately 500 patients with PPCM and 500 apparently healthy pregnant women will be recruited over a 6-month period with follow-up at 3-monthly intervals for 18 months. The objectives of the study are: i. To describe the burden and demographic, social and clinical characteristics of PPCM in Nigeria. ii. To describe the ventricular remodelling and outcomes (rehospitalisation rate, cardio-embolic events and survival) of PPCM in Nigeria. Sub-study: iii. To study the relationship between selenium deficiency, oxidative stress and PPCM in Nigeria. iv. To describe the prevalence of selenium deficiency and its relationship with cardiac function in apparently healthy pregnant women in Nigeria. v. To study the impact of sodium selenite supplementation on cardiac function among selenium deficient PPCM patients who have not recovered left ventricular function at 6 months after the diagnosis. This will be the largest systematic evaluation of PPCM in Nigeria, and it is hoped that the information will assist in developing locally applicable treatment guidelines, policies and interventions for this seemingly deadly disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripartum Cardiomyopathy
Keywords
peripartum cardiomyopathy, Ventricular remodelling, Survival, Selenium, Oxidative stress, Nigeria

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Active Comparator
Arm Description
Oral Sodium Selenite 200 µg/day for 3 months
Arm Title
Control
Arm Type
No Intervention
Arm Description
No treatment
Intervention Type
Drug
Intervention Name(s)
Oral Sodium Selenite 200 µg/day for 3 months
Other Intervention Name(s)
Nature's way Selenium 200mcg
Intervention Description
PPCM patients with selenium deficiency, who have not achieved LV reverse remodelling (LVRR) (LV end-diastolic dimension indexed to body surface area (LVEDDi) ≤33.0 mm/m2) at 6 months after diagnosis.
Primary Outcome Measure Information:
Title
Prevalence of peripartum cardiomyopathy (PPCM) in Nigeria
Description
All participants confirmed to have PPCM presenting to the study centres, as described in PEACE Registry protocol V3.
Time Frame
Over 6 months
Secondary Outcome Measure Information:
Title
Selenium deficiency in PPCM patients and apparently healthy pregnant women in Nigeria
Description
Prevalence of selenium deficiency will be assessed. Serum selenium will be measured as described in PEACE Registry protocol V3. Selenium deficiency will be defined as serum selenium <70μg/L.
Time Frame
At baseline, 3 months, 12 and 18 months of follow up.
Title
Oxidative stress in PPCM patients and apparently healthy pregnant women in Nigeria
Description
Prevalence of oxidative stress will be assessed. Serum malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidise (GPO) and N-terminal pro-B-type natriuretic peptide (NT-BNP) will be measured as described in PEACE Registry protocol V3. Abnormal oxidative stress will be defined as the presence of serum NT-BNP >125pg/mL and ANY of the following: plasma MDA >1.25μmol/L, serum SOD >110ng/mL and plasma GPO >470U/L.
Time Frame
At baseline, 3 months, 12 and 18 months of follow up.
Title
The effect of sodium selenite supplementation on cardiac function among PPCM patients.
Description
PPCM patients with selenium deficiency, left ventricular ejection fraction (LVEF) <35% and/or insignificant left ventricular reverse remodeling (LVRR) at 6 months postpartum, will be offered sodium selenite 200mcg daily for 3 months, in an open-label randomized trial. LVRR would be defined as the presence of both absolute increase in LVEF ≥10.0% and decrease in LV end-diastolic dimension indexed to body surface area (LVEDDi) ≤33.0 mm/m2, while recovered LV systolic function as LVEF ≥55%, during the follow-up. Change in LVEF and LVEDDi will be measured at 6, 12, and 18 months follow up visits, to determine prevalence of LVRR among partipants on selenium treatment and those who will not be on selenium treatment.
Time Frame
18 months
Title
Left Ventricular remodelling in PPCM patients
Description
Change in LVEF and LVEDDi to determine LVRR
Time Frame
At baseline, and 6, 12 and18 months follow up
Title
Right Ventricular (RV) remodelling in PPCM patients
Description
Change in RV fractional area change (RVFAC) of the right ventricle (in cm2), to determine RV reverse remodelling (RVRR). RVRR is defined as RVFAC >35cm2.
Time Frame
At baseline, and 6, 12 and18 months follow up
Title
Rehospitalisation rate
Description
Number of participants who experience hospitalization for any cardiovascular disease during follow up.
Time Frame
18 months
Title
Prevalence of cardio-embolic events
Description
Number of participants who experience stroke, transient ischemic attack or any gangrene during the follow-up period of the study.
Time Frame
18 months
Title
Survival rate
Description
Number of participants who have survived the follow-up period of the study.
Time Frame
18 months

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Confirmed diagnosis of PPCM PPCM patients with HF symptoms at the time of recruitment Asymptomatic pregnant women attending antenatal clinic (ANC) Sub-study: Open-label randomised Trial: Non-pregnant PPCM patients with all of the following: LVEF <35% and/or LVEDDi≤33.0 mm/m2 at 6 months postpartum AND selenium deficiency Written informed consent Exclusion Criteria: Asymptomatic PPCM patients at the time of recruitment PPCM patients who are not expected to survive at least 6 months from recruitment Pregnant women with any medical condition other than PPCM Subjects who are considered not likely to attend follow up reviews regularly, because of lack of patient's and close relative's phone numbers, or long distance from the study centre, etc Refusal or withdrawal of consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kamilu M Karaye, PhD
Organizational Affiliation
Aminu Kano Teaching Hospital, Kano
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aminu Kano Teaching Hospital
City
Kano
ZIP/Postal Code
700233
Country
Nigeria
Facility Name
Aminu Kano Teaching Hospital
City
Kano
Country
Nigeria

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
We intend to publish the results in peer reviewed scientific journals.
Citations:
PubMed Identifier
33087055
Citation
Karaye KM, Sa'idu H, Balarabe SA, Ishaq NA, Sanni B, Abubakar H, Mohammed BL, Abdulsalam T, Tukur J, Mohammed IY. Selenium supplementation in patients with peripartum cardiomyopathy: a proof-of-concept trial. BMC Cardiovasc Disord. 2020 Oct 21;20(1):457. doi: 10.1186/s12872-020-01739-z. Erratum In: BMC Cardiovasc Disord. 2021 Jan 4;21(1):4.
Results Reference
result
PubMed Identifier
33397290
Citation
Karaye KM, Sa'idu H, Balarabe SA, Ishaq NA, Sanni B, Abubakar H, Mohammed BL, Abdulsalam T, Tukur J, Mohammed IY. Correction to: Selenium supplementation in patients with peripartum cardiomyopathy: a proof-of-concept trial. BMC Cardiovasc Disord. 2021 Jan 4;21(1):4. doi: 10.1186/s12872-020-01782-w. No abstract available.
Results Reference
result

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Peripartum Cardiomyopathy in Nigeria Registry

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