Long-Term Lead Chelation Therapy and Progressive Renal Insufficiency

This study has been completed.
Sponsor:
Information provided by:
Chang Gung Memorial Hospital
ClinicalTrials.gov Identifier:
NCT00227409
First received: September 26, 2005
Last updated: October 17, 2006
Last verified: September 2005
  Purpose

Previous study showed repeated lead chelation therapy significant reduced progressive renal insufficiency in patients with chronic renal diseases and high-normal body lead burden in a placebo-controlled, randomized, 2-year clinical trial, even factors that influence progression, such as blood pressure, the presence or absence of hyperlipidemia, and urinary protein excretion were well controlled.Since relative small sample size and short duration of follow-up were noted in the previous study, whether repeated lead chelation therapy could long-term retard the progression of renal insufficiency remains unknown. Hence, we conducted a 51-month placebo-controlled clinical trial to assess the long-term effect of repeated chelation in progressive renal insufficiency of patients with high-normal body lead burden.


Condition Intervention
Urologic Disease
Drug: calcium disodium EDTA (edetate calcium disodium)

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Treatment
Official Title: Long-Term Repeated Lead Chelation Therapy in Non-Diabetic Patients With Chronic Renal Insufficiency and High-Normal Body Lead Burden

Resource links provided by NLM:


Further study details as provided by Chang Gung Memorial Hospital:

Primary Outcome Measures:
  • The primary end point was an increase in serum creatinine to 2 times the base-line value or the need for dialysis.

Study Start Date: November 2001
Estimated Study Completion Date: October 2005
  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients from 18 through 80 years of age who had chronic renal insufficiency were eligible if they had a serum creatinine concentration between 1.5 mg per deciliter (132.6 μmol per liter) and 3.9 mg per deciliter (344.8 μmol per liter), with a decrease in the glomerular filtration rate of less than 5 ml per minute over a period of at least six months
  • Blood pressure less than 140/90 mm Hg
  • A cholesterol level below 240 mg per deciliter
  • Daily protein intake under 1 g per kilogram of body weight
  • No known history of exposure to lead or other heavy metals, and a high-normal body lead burden (between 60 and 600 μg, as measured by EDTA mobilization testing and 72-hour urine collection).

Exclusion Criteria:

  • Patients who have renal insufficiency with a potentially reversible cause, such as malignant hypertension, urinary tract infection, hypercalcemia, or drug-induced nephrotoxic effects
  • Systemic diseases, such as connective-tissue diseases or diabetes mellitus
  • Use of drugs that might alter the course of renal disease, such as nonsteroidal anti-inflammatory agents, steroids, or immunosuppressive drugs
  • Rapidly progressive glomerulonephritis or a high level of 24-hour urinary protein excretion (more than 8 g per day)
  • Previous marked exposure to lead and other metals(lead poisoning or occupational exposure)
  • Drug allergies
  • Absence of informed consent.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00227409

Locations
China, Taiwan
Chang Gung Memorial Hospital
Taipei, Taiwan, China, 105
Sponsors and Collaborators
Chang Gung Memorial Hospital
Investigators
Principal Investigator: Ja-Liang Lin, MD Division of Nephrology, Chang Gung Memorial Hospital
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00227409     History of Changes
Other Study ID Numbers: NMRPG3029, NSC93-2314-B-182A- 079
Study First Received: September 26, 2005
Last Updated: October 17, 2006
Health Authority: Taiwan: Department of Health

Keywords provided by Chang Gung Memorial Hospital:
Repeated chelation therapy
Progressive renal insufficiency
Body lead burden
Long-term outcome
Glomerular filtration rate

Additional relevant MeSH terms:
Kidney Failure, Chronic
Renal Insufficiency, Chronic
Renal Insufficiency
Urologic Diseases
Kidney Diseases
Pentetic Acid
Edetic Acid
Calcium, Dietary
Chelating Agents
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Antidotes
Protective Agents
Physiological Effects of Drugs
Iron Chelating Agents
Anticoagulants
Hematologic Agents
Therapeutic Uses
Bone Density Conservation Agents

ClinicalTrials.gov processed this record on April 14, 2014