Evaluating Iron Protein Succinylate Oral Solution in Treating Chronic Heart Failure and Iron Deficiency

NCT ID: NCT03344523

Last Updated: 2017-11-17

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 600 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-01-31
• Study Completion Date: 2019-12-31

Brief Summary

This study aims to evaluate the effect of standard heart failure therapy plus oral solution with protein succinylate iron compared to placebo on the primary end point of 6 minute walk distance at 24th week in patients with chronic ejection fraction reduction heart failure and iron deficiency.

Detailed Description

This clinical trial was designed as a multicenter, prospective, randomized, double-blind controlled study. Patients were randomly divided into one of two treatment groups:

Control group: standard treatment + placebo（1 bottle orally, twice daily, take orally before meals, duration of treatment 16-24 weeks）.

Test group: standard treatment + Iron protein succinylate oral solution (1 bottle orally, twice daily, take orally before meals, duration of treatment 16-24 weeks）.

Sample size calculation is according to the change of 6 Minute walk distance from the baseline at 24 weeks, it is estimated the mean difference between two groups is 20 meter, standard deviation 80 meter, statistical power 80%, type I error 0.05, follow up loss 15%，estimated total sample size 600.

Conditions

Chronic Heart Failure; Iron-deficiency

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

standard treatment + Iron succinylate

1 bottle orally, twice daily, take orally before meals

Group Type: EXPERIMENTAL

Iron protein succinylate oral solution

Intervention Type: DRUG

Iron protein succinylate oral solution

standard treatment

Intervention Type: OTHER

standard treatment

standard treatment + placebo

1 bottle orally, twice daily, take orally before meals

Group Type: PLACEBO_COMPARATOR

standard treatment

Intervention Type: OTHER

standard treatment

Interventions

Iron protein succinylate oral solution

Iron protein succinylate oral solution

Intervention Type: DRUG

standard treatment

standard treatment

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Sign informed consent form;

2. Between 18 to 80 years old, male or female;

3. Patients with chronic ejection fraction reduction heart failure, has been accepted the medication recommended by the Guidelines for treatment of heart failure in China (2014) for at least 4 weeks (that comply with the following requirements): if there is no contraindications or intolerance, patients should receive the renin angiotensin aldosterone system inhibitors, B blockers, and no dose adjustment within 4 weeks (not including diuretics). For patients who do not follow the guidelines for the use and titration of the renin angiotensin aldosterone system inhibitor and B blocker drugs, the cause should be recorded;

4. LVEF< 40% (determined by Simpson method) (valid for one week before randomization);

5. NYHA heart function II-III Grade;

6. NT-proBNP>400pg/ml, it should be .900pg/ml at atrial fibrillation;

7. Upper limit of hemoglobin: women less than 120g/L, men less than 130g/L. Lower limit of hemoglobin: more than 90g/L for both men and women. Accompanied by Iron deficiency (iron deficiency is defined as serum ferritin<100ug/L, or serum ferritin between 100~300ug/L with transferrin saturation (Tsat) <20%);

8. Capable of 6 Minute walk test.

Exclusion Criteria

1. Patients with significant bleeding: gastrointestinal bleeding, menorrhagia, history of gastrointestinal bleeding and no evidence of gastrointestinal disease healing;

2. History of oral iron supplementation and intolerance;

3. History of acquired iron overload;

4. Exclude if receiving erythropoietin, intravenous iron, transfusion therapy and oral iron (including iron contained in compound vitamins or other compound medicine) ≧75mg/day within 6 weeks before enrollment;

5. Patients in urgent need of blood transfusion;

6. VtaminB12 and/or folate deficiency, unless correctable; and Non-iron deficiency anemia;

7. Severe renal insufficiency（eGFR < 20ml/min/1.73m2, MDRD formula）, renal anemia; or history of kidney dialysis, need of kidney dialysis at present or in 6 months;

8. Chronic liver disease, cirrhosis, active hepatitis, transaminases (increase of alanine aminotransferase and aspartate aminotransferase 3 times above the normal upper limit. Total bilirubin 3 times higher than the normal upper limit);

9. Intestinal diseases which affect iron absorption such as inflammatory bowel disease and chronic pancreatitis;

10. Active infection;

11. History of syncope within 3 months, diagnosed as cardiogenic shock over the past 1 months;

12. Active myocarditis, constrictive pericarditis and other pericardial diseases;

13. Acute decompensated heart failure with unstable hemodynamics;

14. Symptomatic bradycardia or second or third-degree cardiac conduction block with no pacemaker installed;

15. Severe chronic obstructive pulmonary disease, pulmonary heart disease, severe pulmonary vascular disease, pulmonary hypertension caused by autoimmune diseases and any type of severe pulmonary hypertension;

16. Valvular heart disease and congenital heart disease without operation; hypertrophic cardiomyopathy, restricted cardiomyopathy, and other secondary cardiomyopathy;

17. Patients with malignancy;

18. Patients combined with other organ diseases such as hematopoietic system, nervous system, endocrine system like thyroid, and combined with psychosis;

19. There is uncontrolled hypertension, systolic pressure is greater than 180mmHg and/or diastolic pressure is greater than 110mmHg;

20. Heart rate ≥ 130 times/minute before randomization, or malignant ventricular arrhythmia affecting hemodynamic;

21. Neuromuscular disease, disability or other non-cardiac causes influencing the performance of 6 Minute walk test;

22. Occurred within 3 months: acute coronary syndrome, stroke, transient cerebral ischemic attack; cardiac, carotid artery or other major vascular surgery; percutaneous coronary intervention (PCI) or carotid artery angioplasty or coronary bypass surgery and other cardiac surgery; or scheduled for percutaneous intervention and surgery surgical treatment within 6 months;

23. Has been implanted pacemaker/defibrillator (CRT-P/D) of cardiac resynchronization therapy within 6 months, or the intention to implant a similar device within 6 months after randomization;

24. Has been received major surgery within 6 months prior to randomization, or intend to receive major surgical treatment within 6 months;

25. History of heart transplantation or waiting for transplantation or using a left ventricular assist device (LVAD) or a heart transplant intention (waiting for transplantation) or intend to use VAD over the next 6 months;

26. Nursing or pregnant women, or women of childbearing age without contraception, or patients planned pregnancy in 6 months;

27. History of major organ transplant (such as lung, liver, bone marrow, kidney)

28. Patients have been involved or to be involved in other clinical trials within one month;

29. Patients cannot understand the informed consent form or cannot make decisions or of poor compliance;

30. Patients judged as unsuitable for the study and life expectancy less than 1 year by investigators.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Lee's Pharmaceutical Limited

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

2016-ZX02

Identifier Type: -

Identifier Source: org_study_id