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Clinical Trial Details

Trial ID: L1150
Source ID: NCT05807711
Associated Drug: L-Methyl Folate And Methylcobalamine
Title: Efficacy of L-methylfolate and Methylcobalamine in Treating Resistant Hypertension Associated with Elevated Serum Homocysteine in Hemodialysis Patients.
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: End Stage Renal Disease|Hypertension, Renal
Interventions: DRUG: L-Methyl Folate and methylcobalamine
Outcome Measures: Primary: average pre-dialysis blood pressure target of ≤ 140/90 mm Hg or an average post-dialysis blood pressure target of ≤ 130/80 mm Hg, To achieve an average pre-dialysis blood pressure target of ≤ 140/90 mm Hg or an average post-dialysis blood pressure target of ≤ 130/80 mm Hg. This should be parallel to lowering of serum homocysteine compared to baseline values, 3 months | Secondary: myocardial infarction, stroke and cardiovascular events., As a measurement of the prognosis patients will be followed up for the development of myocardial infarction, stroke and cardiovascular events for 3 months., 3 months
Sponsor/Collaborators: Sponsor: Alexandria University
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE4
Enrollment: 51
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2023-04-01
Completion Date: 2024-05-01
Results First Posted:
Last Update Posted: 2025-01-13
Locations: Faculty of Pharmacy, Alexandria University, Alexandria, 21521, Egypt
URL: https://clinicaltrials.gov/show/NCT05807711