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Search / Trial NCT00624208

The Effects of the Anti Nausea Drugs Droperidol and Ondansetron on the Way the Heart Recovers Between Beats

Launched by UNIVERSITY OF BRITISH COLUMBIA · Feb 26, 2008

Trial Information

Current as of September 13, 2025

Completed

Keywords

Randomized Double Blind 4 Group Clinical Interventional Study

ClinConnect Summary

1. Purpose: to examine in detail the effect of droperidol and ondansetron on Tp-e (an ECG measure of dispersion of repolarization); to search with maximum statistical power for a difference in this parameter before and after exposure to this widely used anaesthetic. To investigate the nature of any dose-response relationship between propofol and mean QTc and Tp-e intervals.
2. Hypotheses: 1. H0: mean pre-operative Tp-e = mean intra-operative Tp-e within each group vs. H1: mean pre-operative Tp-e ≠ mean intra-operative Tp-e within each group. 2. H0: mean intra-operative Tp-e group 1 = mean i...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Healthy children (ASA I-II) undergoing procedures that require general anesthesia without pre-medication.
  • Exclusion Criteria:
  • Children with long QT syndrome, a family history of long QT syndrome or taking medication that is known to prolong the QT interval.
  • IV access unobtainable pre-operatively.

About University Of British Columbia

The University of British Columbia (UBC) is a leading research institution located in Vancouver, Canada, renowned for its commitment to advancing health sciences through innovative research and education. As a prominent clinical trial sponsor, UBC leverages its interdisciplinary expertise and state-of-the-art facilities to conduct rigorous clinical studies aimed at improving patient outcomes across various medical fields. The university fosters collaborations with healthcare professionals, industry partners, and community stakeholders to translate research findings into practical applications, thereby contributing to the global advancement of medicine and public health.

Locations

Vancouver, British Columbia, Canada

Patients applied

0 patients applied

Trial Officials

Simon Whyte, MD

Principal Investigator

University of British Columbia

Mark Ansermino, MD

Study Director

University of British Columbia

Shubhayan Sanatani, MD

Study Director

University of British Columbia

Joanne Lim

Study Director

University of British Columbia

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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