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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00555685
Other study ID # FAPESP 2007/04048-7
Secondary ID
Status Completed
Phase Phase 2
First received November 8, 2007
Last updated June 6, 2014
Start date February 2008
Est. completion date December 2010

Study information

Verified date June 2014
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

Patients with decompensated heart failure have high rates of mortality and morbidity despite recent improvements in diagnosis and treatment. Some aspects of their presentation such as renal failure, hyponatremia and congestive phenomena have received special attention, as they are associated with worse prognosis. The infusion of hypertonic saline solution has been tested in different conditions of cardiovascular collapse. Current evidence indicates that the infusion of hypertonic solution in heart failure patients can provide clinical and haemodynamic improvement. The investigators are testing the hypothesis that the infusion of hypertonic solution in association with diuretics may prevent the occurrence of renal dysfunction in patients with decompensated heart failure.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date December 2010
Est. primary completion date February 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age over 18 years old

- Heart failure according to Framingham criteria

- Episode of acute decompensation,with need of in-hospital treatment

- Presence of congestive phenomena

Exclusion Criteria:

- Patient denial

- Left-ventricle ejection fraction over 0,4, as measure by transthoracic echocardiography

- Rheumatic disease

- Restrictive cardiomyopathy

- Alcohol abuse

- Chronic obstructive pulmonary disease

- Cancer

- Pulmonary embolism during the last 6 months

- Surgical procedures or acute illness during the last 30 days

- Chronic or acute infection

- Any other circumstance that may hamper patient prognosis for the next 6 months

- Serum creatine over 3.0mg/dL

- Serum potassium over 5.5 mEqs/L

- Any specific condition associated to the acute episode of decompensation, such as new onset cardiac arrhythmias, heart ischemia, infection, etc.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Intervention

Drug:
NaCl 7,5% (Hypertonic Saline Solution)
Patients in the intervention arm will receive 100ml of NaCl 7,5, twice daily during 3 days
NaCl 0,9%
Patients in the placebo arm will receive 100ml of NaCl 0,9% twice daily during 3 days

Locations

Country Name City State
Brazil Heart Institute of São Paulo University Medical School Sao Paulo SP

Sponsors (2)

Lead Sponsor Collaborator
University of Sao Paulo Fundação de Amparo à Pesquisa do Estado de São Paulo

Country where clinical trial is conducted

Brazil, 

References & Publications (3)

Issa VS, Bacal F, Mangini S, Carneiro RM, Azevedo CH, Chizzola PR, Ferreira SM, Bocchi EA. Hypertonic saline solution for renal failure prevention in patients with decompensated heart failure. Arq Bras Cardiol. 2007 Oct;89(4):251-5. English, Portuguese. — View Citation

Licata G, Di Pasquale P, Parrinello G, Cardinale A, Scandurra A, Follone G, Argano C, Tuttolomondo A, Paterna S. Effects of high-dose furosemide and small-volume hypertonic saline solution infusion in comparison with a high dose of furosemide as bolus in refractory congestive heart failure: long-term effects. Am Heart J. 2003 Mar;145(3):459-66. — View Citation

Rocha-e-Silva M, Poli de Figueiredo LF. Small volume hypertonic resuscitation of circulatory shock. Clinics (Sao Paulo). 2005 Apr;60(2):159-72. Epub 2005 Apr 26. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Occurrence of renal disfunction During hospital admission Yes
Secondary Improvement of hyponatremia During hospital admission No
Secondary Improvement of congestive phenomena During hospital admission No
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