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NCT07589036Completed

Effects of Dioscorea Yam Gruel on Blood Lipid Profiles in PCI Patients With Coronary Heart Disease

Effects of Dioscorea Yam Gruel on Blood Lipid Profiles in PCI Patients With Coronary Heart Disease: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 18 May 2026

Brief summary (registry, in English)

This randomized controlled trial investigated the effects of Dioscorea yam gruel on blood lipid levels in patients with coronary heart disease after percutaneous coronary intervention (PCI). A total of 72 eligible post-PCI patients were randomly assigned to the control group or the intervention group. Patients in the control group received standard post-procedural treatment and care. In addition to this standard regimen, those in the intervention group were provided with approximately 150 g of Dioscorea yam gruel daily as a partial dinner replacement for 12 consecutive weeks. Serum levels of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), and body mass index (BMI) were measured at baseline, and at 8 weeks and 12 weeks of the intervention.

Status (registry)
Completed
Study type
Interventional
Enrollment
72 (actual)
First submitted
5 May 2026
Start date
10 Jan 2024
Primary completion date
15 Mar 2025
Lead sponsor
900th Hospital of PLA Joint Logistic Support Force
NCT number
NCT07589036

What you commit to

  • Study type: Interventional
  • Participants enrolled: 72
  • From 10 Jan 2024 to the primary completion date, 15 Mar 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Complicating with other severe diseases or diseases that affect blood lipid levels, such as malignant tumors, acute cerebrovascular disease, nephrotic syndrome, severe liver disease, Cushing's syndrome, and others

Lab values

  • Low-density lipoprotein cholesterol (LDL-C) level \< 70 mg/dL(\<1.81mmol/L) at screening

Other

  • Pregnancy or lactation
  • Concurrently participating in other dietary or exercise intervention programs

Who the study is looking for

  • Meeting the diagnostic criteria for coronary heart disease (2020 edition)
  • Undergoing percutaneous coronary intervention (PCI)
  • Aged between 18 and 75 years
  • Having been on a stable dose of statin therapy for at least 4 weeks prior to screening
  • Being in a stable clinical condition, conscious, providing informed consent, and participating voluntarily

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
900th Hospital of PLA Joint Logistic Support Force
Coordinator of this site? Confirm its status
FuzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.