Oral dIuretics in Very Intensive Treatment, an Early Intervention in Outpatients With Heart Failure

Heart Failure Clinical Trial

— DIVINE  

Official title:

Oral dIuretics in Very Intensive Treatment, an Early Intervention in Outpatients With Heart Failure. DIVINE STUDY

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03709160
• Other study ID #: 18-1051
• Status: Recruiting
• Phase: Phase 4
• Start date: October 15, 2018
• Est. completion date: October 15, 2019

Study information

• Verified date: October 2018
• Source: Centro en Insuficiencia Cardiaca, Mexico
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In the present study, consecutive patients, older than 18 years, of both genders will be included. The diagnosis of reduced Heart Failure (HfrEF) according to: Clinical pattern, laboratories and Cardiac imaging (ESC criteria). Treatment will be assigned in two groups: Bumetanide and another group will be received Indapamide. Each group received maximum tolerated dose for seven days with Clinical and labs evaluations will be every 48 hrs. (Face-to-face and/or telephone visits). Serum and urinary labs, EKG´s, Echo will be evaluated. Daily in-home register will made. Final points were: Mortality, Urinary failure, Clinical Impairment, Hospital admissions, Oedema. (MUCHO). All patients will be followed for 30 days.

Description:

In selected patients who sign informed consent with decompensation of cardiac failure by water congestion will be allocated in two groups: Bumetanide and the other Indapamide group. Each group will be given the maximum tolerated dose for seven days with clinical evaluations every 48 hours. (Face to face and/or telephone). Clinical variables, ECG and serum and urine laboratories will be assessed finally, patients will follow up for 30 days. To identify endpoints such as: mortality, urinary failure, clinical deterioration, hospital admissions, edema. (MUCHO).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: October 15, 2019
• Est. primary completion date: October 15, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 1. Older over 18 year 2. Both gender. 3. Patients are able to read, write and understand. 4.-Heart failure criteria:a) Clinical signs and symptoms b) serum NTP-proBNP: over 125pg/ml. or serum bnp: over: 35pg/ml. c) Left ventricular ejection fraction under 40% ( By any image study: echocardiogram, Tomography , MRI,Nuclear medicine.) 5. Commitment to participate in the follow-up of the present study.

Exclusion Criteria:

1. Pregnant or lactating women.

2. Patients with deterioration of their clinical condition that warrant rapid attention by the emergency department.

3. Patients with symptomatic hypotension by arterial pressure over; 90/50 mmHg.

4. Symptomatic heart rate disorders: tachycardia greater than 120 beats per minute or bradycardia less than 50 beats per minute.

5. Patients with respiratory impairment: by tachypnea (respiratory rate greater than 22 per min), peripheral oxygen saturation less than 90%.

6. Clinical signs or by methods of pleural effusion image that compromise the ventilatory mechanism.

7. Hormonal thyroid decontrol (thyroid hormone profile outside the reference range)

8. Serum glucose numbers greater than 140mg/DL and/or glycosylated hemoglobin greater than 6.5%.

9. Renal damage characterized by serum creatinine numbers greater than 1.5 mg/DL.

10. Alteration of the hepatic test: serum aspartate aminotransferase and/or serum alanine aminotransferase by levels greater than three times the upper limit of reference.

11. Alterations in serum electrolytes (by sodium greater 135 mmol/L or less 145 mmol; Potassium less than 3.5 mmol/L or higher 5.35 mmol/L)

12. Intolerance or allergy recognized for any diuretic.

13. Comorbidities that prevent the follow-up of treatment: (Alcoholism, drug addiction, psychiatric disorders)

14. Positive serology carriers for Hepatitis (B, C) HIV.

15. Acute myocardial infarction (with and without elevation) in the last three months.

16. History of vascular (ischemic or hemorrhagic) brain disease in the last three months.

17. Carriers of acute inflammatory and/or immunologic disease in the last three months (e.g. Active Lupus etc.)

18. Active myocarditis in the last three months

19. History of Prostatism, or recognized prostatic alterations, that impede voiding flow.

20. Terminal cancer

21. Blunt physical and cognitive deterioration that prevents optimal follow-up.

22. Cultural barriers involving limitation of communication (languages, dialects, reading and writing, etc.).

23. Not to sign informed consent

Related Conditions & MeSH terms

• Congestive Heart Failure
• Heart Failure

Intervention

Drug:
• Bumetanide 1 MG
all patients will be taking the treatment recommended by heart failure guidelines

Locations

Country	Name	City	State
Mexico	Centro de Insuficiencia Cardiaca Instituto Nacional de Cardiologia	Mexico City

Sponsors (1)

Lead Sponsor	Collaborator
Centro en Insuficiencia Cardiaca, Mexico

Country where clinical trial is conducted

Mexico, 

References & Publications (1)

Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JGF, Coats AJS, Falk V, González-Juanatey JR, Harjola VP, Jankowska EA, Jessup M, Linde C, Nihoyannopoulos P, Parissis JT, Pieske B, Riley JP, Rosano GMC, Ruilope LM, Ruschitzka F, Rutten FH, van der Meer P; ESC Scientific Document Group. 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur Heart J. 2016 Jul 14;37(27):2129-2200. doi: 10.1093/eurheartj/ehw128. Epub 2016 May 20. Erratum in: Eur Heart J. 2016 Dec 30;:. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	MORTALITY	HEART FAILURE DEATH, CARDIOVASCULAR DEATH, OTHER DEATH	30 DAY
Secondary	REHOSPITALIZATION	HEART FAILURE REHOSPITALIZATION, CARDIOVASCULAR REHOSPITALIZATION, OTHER REHOSPITALIZATION	30 DAY
Secondary	URINARY FAILURE	RENAL DETERIORATION (GFR < 50%)	30 DAY
Secondary	CLINICAL IMPAIRMENT	FUNCTIONAL CLASS DETERIORATION	30 DAY
Secondary	OEDEMA	ABNORMAL ACCUMULATION OF FLUID (SWOLLEN ANKLE)	30 DAY