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Search / Trial NCT00445055

Evaluation of 2 Doses of Intravenous Droperidol in the Prevention of Postoperative Nausea

Launched by UNIVERSITY HOSPITAL, BORDEAUX · Mar 7, 2007

Trial Information

Current as of May 28, 2025

Terminated

Keywords

Thyroidectomy Nausea Vomiting Droperidol

ClinConnect Summary

* Principal Objective : Our study examined one main question: Are there difference in efficacy between droperidol IV 0.625 mg or 2.5 mg for the treatment or prophylaxis of PONV to surgical patient undergoing thyroid surgery when they receive it 30 min before emergence from general anaesthesia?
* Secondary Objective :

* comparison of the % of patients in every group:

* having a complete control of their nausea
* requiring secondarily the appeal to another anti-emetic treatment in postoperative
* presenting an Adverse event
* Compare score of sedation in ach groups
* Evalu...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Female
  • More than 18 years old
  • Patients scheduled for thyroid surgery
  • Simplified Apfel score ≥ 2
  • ASA score : 1-2
  • Informed consent obtained from the patient
  • Women able to procreate must have a reliable contraceptive method
  • Exclusion Criteria:
  • Age \< 18 years old
  • Male
  • Obesity
  • Has a severe depressive syndrome
  • Pregnancy women
  • Trouble with cardiac rate
  • Alcoholism
  • Contra-indication for Droperidol prescription

About University Hospital, Bordeaux

The University Hospital of Bordeaux is a leading academic medical center dedicated to advancing healthcare through innovative research and clinical excellence. As a prominent sponsor of clinical trials, the institution integrates cutting-edge scientific inquiry with patient care, fostering an environment that encourages collaboration among multidisciplinary teams. With a commitment to improving treatment outcomes and enhancing patient safety, the University Hospital of Bordeaux plays a pivotal role in the development of new therapies and medical technologies, contributing significantly to the global medical community.

Locations

Pessac Cedex, , France

Patients applied

0 patients applied

Trial Officials

Gérard JANVIER, MD

Study Director

University Hospital, Bordeaux

Laure BAUDOUIN, Dr

Principal Investigator

University Hospital, Bordeaux

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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