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Can Alendronate Suppress Calcification and Improve Bone Density in Chronic Peritoneal Dialysis Patients?

Primary Purpose

End-Stage Renal Disease, Osteoporosis

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
alendronate
Sponsored by
National Taiwan University Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-Stage Renal Disease focused on measuring peritoneal dialysis, artery calcification, bone mineral density

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Have received maintenance PD for more than 3 months at National Taiwan University Hospital, Have high CPP level (≧50), and Have chest X-ray proven aortic calcification or coronary artery calcification proven before. Exclusion Criteria: Patients are excluded if they have any one of the following conditions: Had been hospitalized in recent 3 months due to severe comorbid diseases, Are hypersensitive to alendronate or any of its components, Have esophageal diseases Are not able to stand or sit upright for 30 minutes, Have refractory hypocalcemia, or Patients who are pregnant.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    extent of aortic and coronary artery calcification with and without the use of alendronate
    bone mineral density with and without the use of alendronate

    Secondary Outcome Measures

    serum levels of calcium, phosphorus and parathyroid hormone

    Full Information

    First Posted
    December 1, 2005
    Last Updated
    January 2, 2009
    Sponsor
    National Taiwan University Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00261625
    Brief Title
    Can Alendronate Suppress Calcification and Improve Bone Density in Chronic Peritoneal Dialysis Patients?
    Official Title
    Can Alendronate Suppress Aortic and Coronary Artery Calcification and Improve Bone Mineral Density in Chronic Peritoneal Dialysis Patients?
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2008
    Overall Recruitment Status
    Completed
    Study Start Date
    August 2005 (undefined)
    Primary Completion Date
    October 2007 (Actual)
    Study Completion Date
    October 2007 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    National Taiwan University Hospital

    4. Oversight

    5. Study Description

    Brief Summary
    Alendronate is a safe and effective drug for treating osteoporosis in post-menopausal women. However, its safety and efficacy in increasing bone mineral density in chronic peritoneal dialysis (PD) patients have not been investigated. Etidronate, another bisphosphonate, can suppress the extent of coronary artery calcification in chronic hemodialysis patients. The hypothesis of this study is that alendronate can increase bone mineral density and suppress aortic and coronary artery calcification in chronic peritoneal dialysis patients.
    Detailed Description
    Study Design The study is a prospective, randomized cross-over study. Fifty patients will be included. All participants are randomly allocated to either group 1 or group 2. Each group consists of 25 patients. Group 1 patients receive alendronate 70 mg once weekly in the first 24 weeks of the study, while group 2 patients receive the same dose of drug every week in the second 24 weeks. The extent of coronary artery and aortic calcification is evaluated by using multidetector spiral computed tomography, whereas bone mineral density is measured by dual-energy X-ray absorptiometry. Both examinations are performed at week 0, 24 and 48 for each participant. Serum level of calcium should be kept within normal limits and serum level of phosphorus should be kept below 6 mg/dl. Administration of Alendronate One tablet of alendronate (70 mg per tablet) should be swallowed by each patient once every week with water at least 30 minutes before breakfast, beverage or medication of the day during the treatment period. Patients must not lie down for at least 30 minutes after taking the drug. Measurement of Coronary Artery and Aortic Calcification Multidetector spiral computerized tomography (CT) of the chest is performed at week 0, 24 and 48 for each participant to measure the extent of coronary and aortic calcification. Measurement of Bone Density Dual energy X-ray absorptiometry is performed at week 0, 24 and 48 for each participant to measure the density of bone. Demographic and Clinical Characteristics of Patients Patients characteristics such as age and sex are documented. Clinical parameters including body height, body weight, duration of dialysis, calcium concentration of dialysate, and medication under use are recorded. Blood pressure is measured at each clinical visit for 3 times after the patient has sit for at least 15 minutes. Collection of Laboratory Data Fasting serum levels of albumin, phosphorus, calcium, alkaline phosphatase (ALP), intact parathyroid hormone (iPTH) and hemoglobin level of each patient are checked at study entry and once every month. Fasting serum levels of triglyceride, total cholesterol, high-density lipoprotein cholesterol (HDL-chol), low-density lipoprotein cholesterol (LDL-chol), and hypersensitive C-reactive protein (CRP) of each patient are checked at study entry and once every 3 months. Record of Adverse Effects of Alendronate Any adverse effect of alendronate is recorded every month at clinic visit. Compliance of Patients Compliance of the patients is monitored using telephone calls once every week during the treatment period with alendronate.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    End-Stage Renal Disease, Osteoporosis
    Keywords
    peritoneal dialysis, artery calcification, bone mineral density

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    50 (Anticipated)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    alendronate
    Primary Outcome Measure Information:
    Title
    extent of aortic and coronary artery calcification with and without the use of alendronate
    Title
    bone mineral density with and without the use of alendronate
    Secondary Outcome Measure Information:
    Title
    serum levels of calcium, phosphorus and parathyroid hormone

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Have received maintenance PD for more than 3 months at National Taiwan University Hospital, Have high CPP level (≧50), and Have chest X-ray proven aortic calcification or coronary artery calcification proven before. Exclusion Criteria: Patients are excluded if they have any one of the following conditions: Had been hospitalized in recent 3 months due to severe comorbid diseases, Are hypersensitive to alendronate or any of its components, Have esophageal diseases Are not able to stand or sit upright for 30 minutes, Have refractory hypocalcemia, or Patients who are pregnant.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Tze-Wah Kao, Master
    Organizational Affiliation
    National Taiwan University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    34231877
    Citation
    Hara T, Hijikata Y, Matsubara Y, Watanabe N. Pharmacological interventions versus placebo, no treatment or usual care for osteoporosis in people with chronic kidney disease stages 3-5D. Cochrane Database Syst Rev. 2021 Jul 7;7(7):CD013424. doi: 10.1002/14651858.CD013424.pub2.
    Results Reference
    derived

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    Can Alendronate Suppress Calcification and Improve Bone Density in Chronic Peritoneal Dialysis Patients?

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