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Completed

NCT Number: NCT00588965

Effect of Beta-blocker Therapy on QTc Response in Exercise and Recovery in Normal Subjects

Background. In congenital long QT syndrome type 1 (LQT1), episodes of ventricular tachycardia are usually triggered by exercise and can be prevented in most patients by beta-blocker therapy. In addition, LQT1 associated with a normal resting QT interval can be unmasked by the abnormal QT response to exercise testing (failure of the QT interval to shorten normally). Preliminary data from our laboratory show that the exercise QT intervals of patients with LQT1 are partially normalized by beta-blocker therapy. It is still currently not known if beta-blockers modify the QT/heart rate relationship (a primary effect on repolarization) or if the "normalizing" effect is due to the inability of subjects on beta-blockers to attain sufficiently high workloads (due to reduced heart rate) for prolongation to occur. Moreover, the physiologic response of the exercise QT interval to beta-blockers in healthy control subjects is not known.

Objective. The objective of this study is to define the impact of beta-blocker therapy on the QT response to exercise and recovery in normal subjects.

Methods. Approximately 36 healthy adult subjects age-matched to previously studied LQT1 subjects will undergo 1) screening history, 2) two weeks of beta-blocker therapy ending in an exercise test, and 3) two weeks of placebo therapy ending in an exercise test. Beta blocker and placebo will be given in random order in a double-blind fashion. The QT response to exercise and recovery will be compared between drug-free and beta-blocker-treated states. These data will be compared to those previously collected for LQT1 subjects.

Implications. These results will provide new information about the effect of beta-blocker therapy on repolarization parameters in normal subjects, and will provide a context in which to interpret the previous findings that beta-blocker administration modifies the QT response to exercise in LQT1 subjects.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy normal adults, age- and gender-matched to previously studied LQT1 subjects

Exclusion criteria

  • Cardiac disease
  • Diabetes
  • Hypertension
  • Severe allergic reaction
  • Asthma requiring treatment
  • Use of medications other than oral contraceptives, acetaminophen, nonsteroidal anti-inflammatory drugs, or synthroid or other thyroid medications
  • Pregnancy (subjects will be asked if they are pregnant)
  • Inability to sign informed consent

Treatment and study plan

Placebo

Drug

Placebo will be given 1 pill daily for a week, then 2 pills daily, followed by the exercise test.

propranolol LA

Drug

Subjects will receive propranolol LA 80 mg one pill daily for 1 week then 2 pills daily for 1 week followed by exercise test.

Primary outcomes

  1. QTc Response to Exercise on Versus Off Beta-blocker.

    Time frame: 2 weeks on each treatment then exercise test

    To minimize the effect of heart rate on QT, QT was measured at heart rates between 100 and 110 beats per minute during exercise (on and off beta-blocker) and during recovery (on and off beta-blocker).

Secondary outcomes

  1. Tpeak-end Interval (Tpe)

    Time frame: Measured after 2 weeks on each intervention

    Tpeak-end interval was measured at rest, exercise, and recovery on placebo and on propranolol.

Sponsors and collaborators

Lead sponsor

MetroHealth Medical Center

Other

Registry information

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Jan 9, 2008
Registry last updated
Jul 30, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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