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Genetic Determinants of the Hypokalemic and Hyperglycemic Effect of Albuterol Inhalation - Article


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Albuterol Inhaler

Proventil HFA; Proventil Inhaler; Ventolin Inhaler 




Clinical Trial: Genetic Determinants of the Hypokalemic and Hyperglycemic Effect of Albuterol Inhalation

This study is currently recruiting patients.
Verified by Hadassah Medical Organization August 2004

Sponsored by: Hadassah Medical Organization
Information provided by: Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT00162487

Purpose

Several studies have indicated that albuterol administered either intravenously or by inhalation can significantly reduce plasma potassium concentration in patients suffering from chronic renal failure.In conjunction with the decrease in potassium concentration a modest rise in glucose concentration is usually noted. These metabolic effects are characterized by rapid onset occurring as early as 3-5 minutes following salbutamol administration and lasting for at least 1 hour.

The role played by ß2AR polymorphisms in determining the bronchial and vascular response to ß2AR agonist drugs, have been confirmed by several studies.

The purpose of the present study is to examine possible causal relationships between genetically based alteration in the structure of ß2AR and the metabolic effects of inhaled albuterol.

Condition Intervention
Hyperkalemia
Chronic Renal Failure
 Drug: Albuterol (1,200 μg) through metered-dose inhaler

MedlinePlus related topics:  Kidney Failure;   Metabolic Disorders

Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Pharmacokinetics/Dynamics Study

Official Title: Evalauation of β2 Genetic Polymorphisms and the Effect of Albuterol Inhalation on Potassium and Glucose Plasma Concentration.

Further Study Details: 
Primary Outcomes: The extent of decrease in plasma potassium concentration; The extent of increase in plasma glucose concentration; Plasma concentration of albuterol
Expected Total Enrollment:  150

Study start: August 2002

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • patients regularly attending the nephrological clinic or the dialysis unit
  • persistent potassium concentration above 5 mEq/L

Exclusion Criteria:

  1. Patients suffering from active ischemic heart disease
  2. Patient with a recent history of arrhythmia
  3. Patients treated regularly with ß blockers
  4. Patients treated regularly with salbutamol or other ß2AR agonists
  5. Patients suffering from persistent tachycardia (pulse > 100 beats/min)
  6. Patients who are hemodynamically unstable
  7. Patients suffering from any acute illness

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00162487


Israel
      Hadassah Medical Organization, Jerusalem,  91120,  Israel; Recruiting
Arik Tzukert, DMD  00 972 2 6776095    arik@hadassah.org.il 
Hadas Lemberg, PhD  00 972 2 6777572    lhadas@hadassah.org.il 
Yoseph Caraco, MD,  Principal Investigator

Study chairs or principal investigators

Yoseph Caraco, MD,  Principal Investigator,  Hadassah Medical Organization   

More Information

Study ID Numbers:  27-24/08/01
Last Updated:  September 12, 2005
Record first received:  September 11, 2005
ClinicalTrials.gov Identifier:  NCT00162487
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration
ClinicalTrials.gov processed this record on 2005-09-13

Resources



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Page Updated: June 1, 2005
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