SODIC: Dietary Sodium Intake in Acute Heart Failure

Sponsor
University of Sao Paulo (Other)
Overall Status
Completed
CT.gov ID
NCT03722069
Collaborator
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. (Other), Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo (Other)
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Study Details

Study Description

Brief Summary

This study is design to assess two levels of dietary sodium intake in the treatment of patients with Acute Decompensated Heart Failure.

Condition or Disease Intervention/Treatment Phase
  • Other: Low sodium diet
  • Other: Normal sodium diet
N/A

Detailed Description

This study aim at assessing the effect of two levels of dietary sodium intake during seven days in hospitalized patients with Acute Decompensated Heart Failure. It is a prospective cohort, randomized, with blinded intervention groups: low sodium diet (the patients will receive 3 g/day of dietary sodium intake), and normal sodium diet (patients will receive 7 g/day of dietary sodium intake). Besides that, both groups will be submitted to a fluid intake limited to 1000 ml/day.

Study Design

Study Type:
Interventional
Actual Enrollment :
44 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Normal Sodium Diet Preserves Serum Sodium Levels During Treatment of Acute Decompensated Heart Failure
Actual Study Start Date :
Jul 20, 2014
Actual Primary Completion Date :
Aug 20, 2017
Actual Study Completion Date :
Sep 20, 2017

Arms and Interventions

Arm Intervention/Treatment
Other: Low sodium diet

22 patients were randomized to receive 3 g/day of dietary sodium chloride and a limit of fluid intake of 1000 ml/day.

Other: Low sodium diet
Patients received low sodium diet (3g of sodium chloride/day) and a limit of fluid intake of 1000 ml/day.

Other: Normal sodium diet

22 patients were randomized to receive 7 g/day of dietary sodium chloride and a limit of fluid intake of 1000 ml/day.

Other: Normal sodium diet
Patients received normal sodium diet (7g of sodium chloride/day) and a limit of fluid intake of 1000 ml/day.

Outcome Measures

Primary Outcome Measures

  1. Serum sodium level at day 7 [7 days]

    The difference of the absolute value of serum sodium between the groups in the final evaluation.

Secondary Outcome Measures

  1. Occurrence of hyponatremia [on day 7]

    The detection of serum level of sodium bellow 135 mmol/L

  2. Change in body weight [7 days]

    The difference of the absolute value of body weight between the initial and final values.

  3. Change in serum levels of NT-proBNP [7 days]

    The difference of the absolute value of NT-proBNP between the initial and final values, and between groups.

  4. Change in systolic, diastolic and mean blood pressure [7 days]

    The difference of the absolute value of blood pressure between the initial and final values.

  5. Change in heart rate [7 days]

    The difference of the absolute value of heart rate between the initial and final values.

  6. Change in serum levels of creatinine [7 days]

    The difference of the absolute value of creatinine between the initial and final values.

  7. Proportion of patients exhibiting worsening renal function (defined as increased serum creatinine> 0,3 mg / dL) [7 days]

  8. Change in dyspnea sense [7 days]

    Using a visual anologic scale, with values between 0 and 10, where the minimum 0 is the greatest lack of air (worse) and the maximum 10 is the complete breath (better)

  9. Change in well-being sense [7 days]

    Using a visual anologic scale, with values between 0 and 10, where the minimum 0 is the worse you ever felt (worse) and the maximum 10 is feel better than already (better)

  10. Diuretic dosage and other drugs to ADHF during intervention period [7 days]

    What drugs will be used and the quantities.

  11. Rate of hospital readmission [30 days]

  12. Rate of mortality after discharge [30 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with Acute Decompensated Heart Failure diagnosis, filling the Framingham diagnostic criteria, hospitalized at campus Hospital das Clínicas of Ribeirão Preto.
Exclusion Criteria:
  • Creatinine clearance <30 ml / min / 1.73 m²;

  • Acute coronary syndrome;

  • Stroke;

  • Dementia;

  • Severe cognitive impairment;

  • Cancer;

  • Decompensated diabetes mellitus;

  • Severe liver disease;

  • Septic shock or with clinical signs of sepsis;

  • Chronic renal parenchymal disease prior to the start of the study;

  • ADHF secondary to acute renal failure;

  • Nutritional disorders or those who are unable to take oral intake because of vomiting, dysphagia or gastroenteritis.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital das Clínicas de Ribeirão Preto Ribeirao Preto Sao Paulo Brazil 14048-900

Sponsors and Collaborators

  • University of Sao Paulo
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
  • Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

Investigators

  • Principal Investigator: Marcus V Simões, PhD, Medical School of Ribeirao Preto, University of Sao Paulo

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Camila Godoy Fabricio, Master, University of Sao Paulo
ClinicalTrials.gov Identifier:
NCT03722069
Other Study ID Numbers:
  • 2383/2014
First Posted:
Oct 26, 2018
Last Update Posted:
Oct 31, 2018
Last Verified:
Oct 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Camila Godoy Fabricio, Master, University of Sao Paulo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 31, 2018