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Prospective study of folic acid dosage reduction of homocysteine in H-type hypertension based on MTHFR genotyping accuracy

Prospective study of folic acid dosage reduction of homocysteine in H-type hypertension based on MTHFR genotyping accuracy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061736
Enrollment
Unknown
Registered
2022-07-01
Start date
2022-07-15
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

H- hypertension

Interventions

accurate group:Based on the appropriate dose of folic acid according to the genotype of the patient, the pharmacist will conduct regular follow-up visits in accordance with the expert Consensus on Fam
Regular group:The clinician gave folic acid dose according to clinical experience, pharmacists did not follow up.

Sponsors

Changzhi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with H type hypertension; 2. Be able to understand the purpose of the test and sign the informed consent voluntarily; 3. The patients were between 18-75 years old, with no gender limitation.

Exclusion criteria

Exclusion criteria: 1. Patients under the age of 18; 2. Patients who have participated in other clinical research projects; 3. Long-term use of anticoagulant drugs (such as atrial fibrillation, valve replacement, chronic obstructive pulmonary disease, etc.); 4. There are obvious other abnormal signs, laboratory tests and clinical diseases, according to the judgment of the investigator, are not suitable to participate in the investigator; 5. Patients with malignant tumors, genetic diseases and autoimmune diseases; 6. Patients with severe mental illness or inability to express their wishes; 7. People with allergic constitution, or people known to be allergic to therapeutic drugs; 8. Pregnant or lactating women; 9. Patients who are taking enalapril folic acid tablets or regular folic acid tablets; 10. Patients who are unwilling to fill in informed consent, or are unwilling to accept follow-up visits, or have poor compliance.

Design outcomes

Primary

MeasureTime frame
HCY LEVEL;MTHFR Genetype;

Secondary

MeasureTime frame
Laboratory examination;Adverse events;

Countries

China

Contacts

Public ContactChunxia Hou
yjk2033901@126.com+86 13593266883

Outcome results

None listed

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