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Dapagliflozin in Diabetic Patients (Type 2) With Decompensated Heart Failure

Primary Purpose

Heart Failure

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Dapagliflozin
insulin
Sponsored by
Assiut University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diabetic patient type 2 with history of chronic heart failure(HFrEF) ,there is no prespecified inclusion criterion with respect to heart failure etiology and/or ejection fraction.

Exclusion Criteria:

  1. Other etiologies of fluid overload different from heart failure.
  2. Hyponatremia: Sodium level below 125mmol/l
  3. Unstable patients: acute coronary syndrome, cardiogenic shock .
  4. Patients requiring inotropic agents or renal dialysis.
  5. Pregnancy or breastfeeding period.
  6. sever hepatic disease
  7. GFR is less than 45 mL/min/1.73 m² .
  8. Patient with diabetic ketoacidosis or non ketotic hyperosmolar.

Sites / Locations

  • Assiut University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Dapagliflozin group

Placebo group

Arm Description

50 patients will receive Dapagliflozin plus insulin (if needed) and Diuretics plus conventional heart failure measures.

50 patients will receive insulin for control of blood sugar plus diuretics and anti-failure measures.

Outcomes

Primary Outcome Measures

Changes in body weight measurement (Diuresis effect.)
Diuretic response will be measured by weight loss
Diuresis effect.
Diuretic response will be measured by net fluid loss per mg .

Secondary Outcome Measures

Renal function
Renal function is assessed with the serum creatinine level. Worsening renal function is defined as an increase in the serum creatinine level of more than 0.3 mg/dl at any time during hospitalization
Patient-reported dyspnea will be assessed with the use five point Linker scale

Full Information

First Posted
May 9, 2020
Last Updated
February 15, 2022
Sponsor
Assiut University
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1. Study Identification

Unique Protocol Identification Number
NCT04385589
Brief Title
Dapagliflozin in Diabetic Patients (Type 2) With Decompensated Heart Failure
Official Title
Safety and Efficacy of Adding Dapagliflozin and Furosemide in Diabetic Patients (Type 2) With Decompensated Heart Failure With Reduced Ejection Fraction (HFrEF)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
December 15, 2020 (Actual)
Study Completion Date
December 20, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assiut University

4. Oversight

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

5. Study Description

Brief Summary
We hypothesize that Dapagliflozin could improve the diuretic response in diabetic patients with acute decompensated heart failure owing to its diuretic effect in addition to improvement of blood glucose level without remarkable effect on kidney function or electrolytes.
Detailed Description
The study will include 100 diabetic patients type 2 patients who will be admitted to care unit with decompensated heart failure.50 patient will receive Dapagliflozin plus insulin (if needed) and Diuretics plus conventional heart failure measures ,the other group will receive insulin for control of blood sugar plus diuretics and anti-failure measures. Inclusion Criteria: Diabetic patient type 2 with history of chronic heart failure(HFrEF) ,there is no specified inclusion criterion with respect to heart failure etiology and/or ejection fraction. Age more than 18 years Admission for acute decompensated heart failure The patient already on an oral loop diuretic for at least 1 month before admission, at a dose between 40 mg and 80 mg daily in the case of furosemide and an equivalent dose in the case of a different loop diuretic (20 mg of Torsemide will be considered to be equivalent to 40 mg of furosemide. Exclusion Criteria: Other etiologies of fluid overload different from heart failure. Hyponatremia: Sodium level below 125mmol/l Unstable patients: acute coronary syndrome, cardiogenic shock . Patients requiring inotropic agents or renal dialysis. Pregnancy or breastfeeding period. sever hepatic disease GFR (Glomerular Filtration Rate) is less than 45 mL/min/1.73 m² . Patient with diabetic ketoacidosis or non ketotic hyperosmolar. Treatment arm. The patients will receive: Loop diuretics. Diuretics should be administered at doses sufficient to achieve optimal volume status and relieve congestion without inducing an excessively rapid reduction in intravascular volume. furosemide will be given I.V either by continuous infusion or blouses Antifailure treatment: (Angiotensin converting enzyme inhibitors or Angiotensin II Receptor Blockers, Beta Blockers,Mineralocorticoid Receptor Antagonists, Ivabradine, or others will be individualized according to the patient condition. Dapagliflozin: will be given in a dose of 10mg once daily ( GFR is more than 45 mL/min/1.73 m²) . In Mild or moderate hepatic disease: No dosage adjustment required In Severe hepatic disease: will not be used. Insulin. Insulin therapy should be initiated if blood glucose levels is ≥180 mg/dL (10.0 mmol/L) after initiation of Dapagliflozin treatment. Once insulin therapy is started, a target glucose range of 140-180 mg/dL (7.8-10.0 mmol/L) is recommended The use of subcutaneous rapid- or short-acting insulin before meals or every 4-6 h will be given to correct hyperglycemia according to sliding scale chart. Control arm. The patients will be given Loop diuretics. Anti-failure treatment. Insulin. All the patients will undergo: Complete echo assessment. ECG on admission and daily. Monitoring:24 hours ECG ,Oxygen saturation and blood pressure monitoring. Complete blood count ,blood urea,serum creatinine,blood sugar,electrolytes ,liver function will be measured on admission Blood sugar ,urea,creatinine,Na, K will be measured daily along the whole days of admission. Follow up parameters Diuresis :24-hour diuresis will be quantified every 24 hours (during hospitalization) from the 1st day until last day of admission. diuretic response will be measured by weight loss and net fluid loss per mg . Changes in body weight measurements: the mean of weight lost every 24 hours and the total weight lost from baseline to the last day of hospitalization Renal function will be determined every 24 hours (during hospitalization) from the date of admission until the date of discharge. Renal function is assessed with the serum creatinine level. Worsening renal function is defined as an increase in the serum creatinine level of more than 0.3 mg/dl at any time during hospitalization Electrolyte levels (sodium and potassium) will be determined every 24 hours (during hospitalization) from the date of admission until the date of discharge. Electrolyte levels are assessed with the serum sodium and potassium levels. Patient-reported dyspnea : Patient-reported dyspnea is assessed every 24 hours (during hospitalization) from the date of admission until the date of discharge. Patient-reported dyspnea will be assessed with the use five point Linker scale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Sequential Assignment
Model Description
The study will include 100 diabetic patients type 2 patients who will be admitted to care unit with decompensated heart failure.50 patient will receive Dapagliflozin plus insulin (if needed) and Diuretics plus conventional heart failure measures ,the other group will receive insulin for control of blood sugar plus diuretics and anti-failure measures.
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dapagliflozin group
Arm Type
Active Comparator
Arm Description
50 patients will receive Dapagliflozin plus insulin (if needed) and Diuretics plus conventional heart failure measures.
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
50 patients will receive insulin for control of blood sugar plus diuretics and anti-failure measures.
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin
Other Intervention Name(s)
SGLT-2 inhibitors
Intervention Description
Patient will receive oral Dapagliflozin then monitoring of its efficacy on heart failure symptoms and outcome.
Intervention Type
Drug
Intervention Name(s)
insulin
Intervention Description
insulin
Primary Outcome Measure Information:
Title
Changes in body weight measurement (Diuresis effect.)
Description
Diuretic response will be measured by weight loss
Time Frame
Days of admission (3-5 days)
Title
Diuresis effect.
Description
Diuretic response will be measured by net fluid loss per mg .
Time Frame
Days of admission (3-5 days)
Secondary Outcome Measure Information:
Title
Renal function
Description
Renal function is assessed with the serum creatinine level. Worsening renal function is defined as an increase in the serum creatinine level of more than 0.3 mg/dl at any time during hospitalization
Time Frame
Days of admission (3-5 days)
Title
Patient-reported dyspnea will be assessed with the use five point Linker scale
Time Frame
Days of admission (3-5 days)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diabetic patient type 2 with history of chronic heart failure(HFrEF) ,there is no prespecified inclusion criterion with respect to heart failure etiology and/or ejection fraction. Exclusion Criteria: Other etiologies of fluid overload different from heart failure. Hyponatremia: Sodium level below 125mmol/l Unstable patients: acute coronary syndrome, cardiogenic shock . Patients requiring inotropic agents or renal dialysis. Pregnancy or breastfeeding period. sever hepatic disease GFR is less than 45 mL/min/1.73 m² . Patient with diabetic ketoacidosis or non ketotic hyperosmolar.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ayman Ibrahem, MD
Organizational Affiliation
Assiut University
Official's Role
Study Director
Facility Information:
Facility Name
Assiut University
City
Assuan
ZIP/Postal Code
71515
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32377235
Citation
Ohara K, Masuda T, Morinari M, Okada M, Miki A, Nakagawa S, Murakami T, Oka K, Asakura M, Miyazawa Y, Maeshima A, Akimoto T, Saito O, Nagata D. The extracellular volume status predicts body fluid response to SGLT2 inhibitor dapagliflozin in diabetic kidney disease. Diabetol Metab Syndr. 2020 May 1;12:37. doi: 10.1186/s13098-020-00545-z. eCollection 2020.
Results Reference
background
PubMed Identifier
32364032
Citation
Elsisi GH, Anwar MM, Khattab M, Elebrashy I, Wafa A, Elhadad H, Awad M, Carapinha JL. Budget impact analysis for dapagliflozin in type 2 diabetes in Egypt. J Med Econ. 2020 Aug;23(8):908-914. doi: 10.1080/13696998.2020.1764571. Epub 2020 May 28.
Results Reference
background
PubMed Identifier
32361851
Citation
Linden K, Mailey J, Kearney A, Menown IBA. Advances in Clinical Cardiology 2019: A Summary of Key Clinical Trials. Adv Ther. 2020 Jun;37(6):2620-2645. doi: 10.1007/s12325-020-01355-5. Epub 2020 May 2.
Results Reference
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PubMed Identifier
32360273
Citation
Cappetta D, De Angelis A, Ciuffreda LP, Coppini R, Cozzolino A, Micciche A, Dell'Aversana C, D'Amario D, Cianflone E, Scavone C, Santini L, Palandri C, Naviglio S, Crea F, Rota M, Altucci L, Rossi F, Capuano A, Urbanek K, Berrino L. Amelioration of diastolic dysfunction by dapagliflozin in a non-diabetic model involves coronary endothelium. Pharmacol Res. 2020 Jul;157:104781. doi: 10.1016/j.phrs.2020.104781. Epub 2020 Apr 28.
Results Reference
background
PubMed Identifier
34041280
Citation
Kasem SM, Saied GM, Hegazy ANM, Abdelsabour M. Impact of Acute Insulin Resistance on Myocardial Blush in Non-Diabetic Patients Undergoing Primary Percutaneous Coronary Intervention. Front Cardiovasc Med. 2021 May 10;8:647366. doi: 10.3389/fcvm.2021.647366. eCollection 2021.
Results Reference
derived
PubMed Identifier
33426003
Citation
Ibrahim A, Ghaleb R, Mansour H, Hanafy A, Mahmoud NM, Abdelfatah Elsharef M, Kamal Salama M, Elsaughier SM, Abdel-Wahid L, Embarek Mohamed M, Ibrahim AK, Abdel-Galeel A. Safety and Efficacy of Adding Dapagliflozin to Furosemide in Type 2 Diabetic Patients With Decompensated Heart Failure and Reduced Ejection Fraction. Front Cardiovasc Med. 2020 Dec 7;7:602251. doi: 10.3389/fcvm.2020.602251. eCollection 2020.
Results Reference
derived

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Dapagliflozin in Diabetic Patients (Type 2) With Decompensated Heart Failure

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