Gender Influence on Torsadogenic Actions of Droperidol.
NCT ID: NCT03944681
Last Updated: 2022-11-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
50 participants
INTERVENTIONAL
2019-04-23
2020-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
It has been known, on the basis of research, that females have been more potent to torsadogenic actions of pharmacological agents than males. That could be related to estrogen influence on ECG parameters, which had been proven on animal model. It hasn't been investigated, whether gender is an important factor when considering droperidol's torsadogenic potential.
The aim of this study is to answer a hypothesis, that women are more potent to torsadogenic actions of droperidol in comparison with men.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Role of Droperidol in Postoperative Vomiting
NCT00702442
Drug and Dose Adjustment in Preventing Postoperative Nausea and Vomiting
NCT04719741
Akathisia in Post Operative Outpatients Surgery
NCT01942343
Evaluation of 2 Doses of Intravenous Droperidol in the Prevention of Postoperative Nausea
NCT00445055
Comparison Between Ondansetron 8 mg and Lidocain 40 mg in Preventing Pain Due to Propofol Injection
NCT03134612
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Droperidol group
Droperidol (Xomolix, Kyowa Kirin) 1.25 mg i.v. bolus
Droperidol Injectable Solution
An electrocardiogram analysis in: 5,10,15,20 minutes after injection of 1.25 mg of droperidol used as PONV prophylaxis.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Droperidol Injectable Solution
An electrocardiogram analysis in: 5,10,15,20 minutes after injection of 1.25 mg of droperidol used as PONV prophylaxis.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* ASA (American Society of Anaesthesiologists) physical status 1 and 2
Exclusion Criteria
* ASA (American Society of Anaesthesiologists) physical status 3 and more
* admittance of repolarisation affecting drugs like: antiarrhythmics (Williams group I-IV), psychotropics, macrolides, antireflux drugs
* ischaemic heart disease
* cardiac failure NYHA (Hew York Heart Association) 1 and more
* congenital or acquired heart defects
* arrhythmias in anamnesis
* hormonal contraception,
* postmenopausal
* neoplasms
18 Years
45 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Medical University of Gdansk
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Radosław Owczuk
Clinical Professor, Head of Department of Anaesthesiology and Intensive Care
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Radoslaw Owczuk, Professor
Role: PRINCIPAL_INVESTIGATOR
Medical University of Gdansk
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Medical University of Gdansk
Gdansk, , Poland
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
KB01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.