Perioperative nutritional treatment and effect evaluation of patients with coronary heart disease after PCI

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200057618

Enrollment

Unknown

Registered

2022-03-15

Start date

2022-03-01

Completion date

Unknown

Last updated

2023-10-30

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

Conditions

Coronary heart disease (CHD)

Interventions

Experimental group:Oral nutrients

Control group:No

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-90 years; 2. The patient was diagnosed with coronary atherosclerotic heart disease and cardiac function grade IV or below; 3. Inpatients who had no contraindications to interventional surgery and planned to undergo interventional surgery.

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, lung, liver and kidney insufficiency, or poor systemic condition who cannot tolerate surgery; 2. Patients with cardiac pacemakers; 3. Pregnant or lactating women; 4. Patients who refuse interventional surgery and choose conservative treatment; 5. Have serious cognitive impairment or mental illness, unable to cooperate with the research; 6. Patients who do not agree or refuse to use nutritional intervention programs.

Design outcomes

Primary

Measure	Time frame
Human composition analysis;B type natriuretic peptide, BNP;	—

Countries

China

Contacts

Public ContactWang Jian

The Second Affiliated Hospital of Army Medical University

wangjian_1996@aliyun.com+86 23 68774836

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026