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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00953914
Other study ID # 04471
Secondary ID
Status Completed
Phase N/A
First received August 4, 2009
Last updated July 6, 2011
Start date March 2005
Est. completion date May 2010

Study information

Verified date July 2011
Source Hospital de Clinicas de Porto Alegre
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

The purpose of the study is to determine if pyridostigmine bromide improves heart rate variability of type 2 diabetes mellitus subjects with cardiovascular autonomic neuropathy.


Description:

The reduced heart rate variability is associated with increased risk of death in patients with diabetes mellitus. Cholinesterase inhibition with pyridostigmine bromide increases heart rate variability in normal individuals and congestive heart failure subjects but its effects on patients with diabetes mellitus is unknown. Based on those evidences, we will test if the short-term administration of pyridostigmine bromide increases heart rate variability in patients with diabetes mellitus.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date May 2010
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- diabetes mellitus

Exclusion Criteria:

- myocardial infarction

- acute ischemic syndromes

- second or third degree atrioventricular block

- active alcoholism

- thyroid dysfunction

- chronic obstructive pulmonary disease

- history of intolerance to pyridostigmine.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Pyridostigmine
Pills containing 30 mg of Pyridostigmine will be orally administered 3 times daily for 1 day.
Placebo
If subject is randomized to placebo, placebo pills will give 30 mg orally 3 times daily for 2 days

Locations

Country Name City State
Brazil Hospital de Clínicas de Porto Alegre Porto Alegre Rio Grande do Sul

Sponsors (1)

Lead Sponsor Collaborator
Hospital de Clinicas de Porto Alegre

Country where clinical trial is conducted

Brazil, 

References & Publications (1)

Behling A, Moraes RS, Rohde LE, Ferlin EL, Nóbrega AC, Ribeiro JP. Cholinergic stimulation with pyridostigmine reduces ventricular arrhythmia and enhances heart rate variability in heart failure. Am Heart J. 2003 Sep;146(3):494-500. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary autonomic modulation assessed by heart rate variability 1 day No
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