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Effect of Glutamine on Cardiac Reserve in Healthy Individuals and Patients with Heart Failure

Effect of Glutamine Supplementation on Cardiac Reserve in Healthy Individuals and Patients with Heart Failure

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082676
Enrollment
Unknown
Registered
2024-04-03
Start date
2024-09-02
Completion date
Unknown
Last updated
2026-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

heart failure

Interventions

Group A1:Healthy participants were administered placebo beverages (10 g of glutamine powder dissolved in 500 mL of lemon water) before the first stress test, and after a 7-day washout period, they pro
Group B1:Healthy participants were administered placebo beverages (500 mL of lemon water) before the first stress test, and after a 7-day washout period, they proceeded to the second stress test. Befo
Group A2:Heart failure patients were administered placebo beverages (10 g of glutamine powder dissolved in 500 mL of lemon water) before the first stress test, and after a 7-day washout period, they p
Group B2:Heart failure patients were administered placebo beverages (500 mL of lemon water) before the first stress test, and after a 7-day washout period, they proceeded to the second stress test. Be

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: I. Healthy Participants: 1. Age >=18 years, inclusive of both males and females (aged between 18 and 60 years old) 2. In good health with no history of cardiovascular diseases 3. Signed informed consent obtained and willing to undergo combined cardiopulmonary exercise testing and exercise stress echocardiography II. Chronic Heart Failure Patients: 1. Age >=18 years 2. Classified as NYHA Functional Class II to III 3. Hospitalized due to heart failure within the past 2 years or demonstrated elevated NT-proBNP or BNP levels within the last 3 months: For sinus rhythm: NT-proBNP >=300 pg/mL; For atrial fibrillation: NT-proBNP >=600 pg/mL 4. Evidence of left ventricular systolic dysfunction or diastolic dysfunction based on echocardiography within the past year: LVEF =50% with at least one of the following indicators of left ventricular diastolic dysfunction: A. Enlarged left atrium: transverse diameter >=38mm. B. Increased left ventricular wall thickness: septum or posterior wall >=11mm, or Left Ventricular Mass Index (LVMI) >=115 g/m² (for males)/ 95 g/m² (for females). C. Elevated left ventricular filling pressure: E/e’ ratio >=13, or mean e’ <9 cm/s 5. Stable chronic heart failure patients who have been under optimal Guideline-Directed Medical Therapy (GDMT) as determined by the investigator for at least 4 weeks, with no changes in heart failure medications (except diuretics) dosage within the last 2 weeks 6. Signed informed consent obtained and willing to undergo combined cardiopulmonary exercise testing and exercise stress echocardiography.

Exclusion criteria

Exclusion criteria: 1. Severe heart failure patients with either LVEF =3 times the Upper Limit of Normal (ULN), or alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >=3 times ULN. 7. Patients with resting heart rate consistently >90 bpm or 100 beats per minute).

Design outcomes

Primary

MeasureTime frame
Peak cardiac output;

Secondary

MeasureTime frame
Peak VO2;Peak heart rate;Peak LVEF;

Countries

China

Contacts

Public ContactJingyi Ren

China-Japan Friendship Hospital

renjingyi1213@hotmail.com+86 186 0019 5099

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026