Using α-ketoglutarate to treat hypertension

The Effects of α-ketoglutarate on Blood Pressure and Endothelial Function in Hypertensive Patients

NA · First Affiliated Hospital, Sun Yat-Sen University · NCT06445244

This study is testing if taking α-ketoglutarate can help people with high blood pressure feel better and improve their blood vessel health.

Quick facts

PhaseNA
Study typeInterventional
Enrollment30 (estimated)
Ages18 Years to 65 Years
SexAll
SponsorFirst Affiliated Hospital, Sun Yat-Sen University (other)
Locations1 site (Guangxi, Nanning)
Trial IDNCT06445244 on ClinicalTrials.gov

What this trial studies

This study investigates the effects of α-ketoglutarate supplementation on patients with primary hypertension and vascular dysfunction. Participants will receive 1000mg capsules of α-ketoglutarate along with lifestyle modification guidance. The aim is to reduce blood pressure and improve endothelial function, potentially reversing the pathological changes associated with hypertension. The study targets individuals aged 18 to 65 who meet specific blood pressure criteria and have not used certain medications recently.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18 to 65 with primary hypertension and vascular dysfunction.

Not a fit: Patients with secondary hypertension or those currently using medications that affect blood pressure will not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a novel approach to managing hypertension and preventing cardiovascular diseases.

How similar studies have performed: While the approach of using α-ketoglutarate is relatively novel, recent clinical trials have shown promising results in related areas.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1、 Primary hypertension (office blood pressure: systolic blood pressure 130~159 mmHg and/or diastolic blood pressure 80~99 mmHg, which meets the diagnostic criteria of hypertension class 1 of 2018AHA hypertension guidelines) and accompanied by vascular dysfunction (FMD\<5%); 2、 Age between 18 and 65 years old; 3, Not using any drugs and dietary supplements that affect blood pressure and vascular endothelial function in the last 3 months, mainly including antihypertensive, lipid-lowering, hypoglycemic drugs and natural plant extract antioxidants; 4、 Voluntarily sign the informed consent form after fully understanding the purpose and process of the study, disease characteristics, drug effects, methods of relevant examinations, and potential risks/benefits of the study.

Exclusion Criteria:

1. Presence of secondary hypertension (those who have been diagnosed with secondary hypertension in the past and have not been definitively cured, and if secondary hypertension is suspected, a complete examination is required to exclude common secondary hypertension, including renal hypertension (renal parenchymal lesions, renal artery stenosis), primary aldosteronism, Cushing's syndrome, pheochromocytoma, aortic constriction, and severe obstructive sleep apnea);
2. Acute myocardial infarction within the past 6 months;
3. recent history of stroke (within 6 months); 4, Dilated heart disease, hypertrophic cardiomyopathy, rheumatic heart disease, congenital heart disease, severe heart valve disease (severe valve stenosis and or regurgitation);

5\. patients with a combination of serious physical illnesses, such as cancer; 6, Severe hepatic or renal dysfunction (ALT and or AST) ≥ 3 times the upper limit of normal, or dialysis end-stage renal disease or eGFR \< 30 ml/min/1.73 m2, or serum creatinine \> 2.5 mg/dL \[\> 221 μmol/L\]); 7. Symptomatic heart failure or reduced left ventricular ejection fraction (\<40%) within the past 6 months; 8. History of hypersensitivity to the study drug or to its components after administration; 9. Participating in other clinical studies; 10. Patients with mental illness who are unable to cooperate; 11, Pregnant, lactating or expectant mothers;

Where this trial is running

Guangxi, Nanning

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Hypertension

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.