UnknownPhase 3Other

Comparison of Three Different Strategies to Prevent Propofol Induced Pain During Infusion

Sponsored by Hospices Civils de Lyon

NCT ID
NCT00146926
Target Enrollment
200 participants
Start Date
2005-09

About This Study

Propofol is a popular intravenous drug to induce anesthesia but it causes local pain with an incidence between 40 and 90%. Three different strategies to prevent propofol induced pain will be studied compared with placebo. Pain will be scored with a four-point scale.

Conditions Studied

Induction of Total Intravenous General Anesthesia

Interventions

  • kétamine 20mg
  • ephedrine 3mg
  • lidocaine 40mg

Eligibility

Age:18 Years - 75 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

Healthy adults (ASA 1-2) for scheduled surgery under general anesthesia with propofol

Exclusion Criteria:

* pregnant
* sedative or analgesic drug 24h before surgery
* allergy with drug used in the study
* difficulty of communication
* absence of informed written consent

Study Locations (1)

Grégoire CHATAIN
Lyon, France

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source