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A randomized controlled trial for exploring the efficacy of folic acid and Vitamin B in lowering hyperhomocystinemia in patients with chronic renal failure and improving left ventricular hypertrophy

A randomized controlled trial for exploring the efficacy of folic acid and Vitamin B in lowering hyperhomocystinemia in patients with chronic renal failure and improving left ventricular hypertrophy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17013161
Enrollment
Unknown
Registered
2017-10-30
Start date
2017-11-01
Completion date
Unknown
Last updated
2017-11-06

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

Conditions

chronic renal failure

Interventions

Experimental group:Folic Acid Tablets 15 mg/d+ vitamin B6 tablets 60mg/d+ vitamin B12 tablets 0.5mg/d
Control group:placebo

Sponsors

The Third Affiliated Hospital, Sun Yat-Sen University, Yuedong Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Serum creatinine levels ranged from 1.5 to 5 mg/dl (133 to 442 mol/L) and creatinine clearance ranged from 20 to 70 ml/1.73 m2, and within three months the change was less than 30%. No urinary tract infection or obvious heart failure (New York Heart Association class III or IV]), all patients were given drug eluting for 6 weeks, and stopped taking folic acid, vitamin B6 and vitamin B12 drugs.;Inclusion criteria: Serum creatinine levels ranged from 1.5 to 5 mg/dl (133 to 442 mol/L) and creatinine clearance ranged from 20 to 70 ml/1.73 m2, and within three months the change was less than 30%. No urinary tract infection or obvious heart failure (New York Heart Association class III or IV]), all patients were given drug eluting for 6 weeks, and stopped taking folic acid, vitamin B6 and vitamin B12 drugs.;Inclusion criteria: Serum creatinine levels ranged from 1.5 to 5 mg/dl (133 to 442 mol/L) and creatinine clearance ranged from 20 to 70 ml/1.73 m2, and within three months the change was less than 30%. No urinary tract infection or obvious heart failure (New York Heart Association class III or IV]), all patients were given drug eluting for 6 weeks, and stopped taking folic acid, vitamin B6 and vitamin B12 drugs.;Inclusion criteria: Serum creatinine levels ranged from 1.5 to 5 mg/dl (133 to 442 mol/L) and creatinine clearance ranged from 20 to 70 ml/1.73 m2, and within three months the change was less than 30%. No urinary tract infection or obvious heart failure (New York Heart Association class III or IV]), all patients were given drug eluting for 6 weeks, and stopped taking folic acid, vitamin B6 and vitamin B12 drugs.;Inclusion criteria: Serum creatinine levels ranged from 1.5 to 5 mg/dl (133 to 442 mol/L) and creatinine clearance ranged from 20 to 70 ml/1.73 m2, and within three months the change was less than 30%. No urinary tract infection or obvious heart failure (New York Heart Association class III or IV]), all patients were given drug eluting for 6 weeks, and stopped taking folic acid, vitamin B6 and vitamin B12 drugs.

Exclusion criteria

Exclusion criteria: (1) have received renal replacement therapy; (2) selected within 1 months before the occurrence of infection; (3) acute cardiovascular events in 1 months before; (4) the use of hormone or immunosuppressant; (5) with malignant tumor, mental illness or pregnancy.;Exclusion criteria: (1) have received renal replacement therapy; (2) selected within 1 months before the occurrence of infection; (3) acute cardiovascular events in 1 months before; (4) the use of hormone or immunosuppressant; (5) with malignant tumor, mental illness or pregnancy.;Exclusion criteria: (1) have received renal replacement therapy; (2) selected within 1 months before the occurrence of infection; (3) acute cardiovascular events in 1 months before; (4) the use of hormone or immunosuppressant; (5) with malignant tumor, mental illness or pregnancy.;Exclusion criteria: (1) have received renal replacement therapy; (2) selected within 1 months before the occurrence of infection; (3) acute cardiovascular events in 1 months before; (4) the use of hormone or immunosuppressant; (5) with malignant tumor, mental illness or pregnancy.;Exclusion criteria: (1) have received renal replacement therapy; (2) selected within 1 months before the occurrence of infection; (3) acute cardiovascular events in 1 months before; (4) the use of hormone or immunosuppressant; (5) with malignant tumor, mental illness or pregnancy.

Design outcomes

Primary

MeasureTime frame
homocysteine;left ventricular hypertrophy;

Countries

China

Contacts

Public ContactHongyong LIU;Hongyong LIU;Hongyong LIU;Hongyong LIU;Hongyong LIU ;;;;

The Third Affiliated Hospital, Sun Yat-Sen University, Yuedong Hospital;The Third Affiliated Hospital, Sun Yat-Sen University, Yuedong Hospital;The Third Affiliated Hospital, Sun Yat-Sen University, Yuedong Hospital;The Third Affiliated Hospital, Sun Yat-Sen University, Yuedong Hospital;The Third Affiliated Hospital, Sun Yat-Sen University, Yuedong Hospital

13823850589@139.com;13823850589@139.com;13823850589@139.com;13823850589@139.com;13823850589@139.com+86 13823850589;+86 13823850589;+86 13823850589;+86 13823850589;+86 13823850589

Outcome results

None listed

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