MedTrace Logo

Effect of Valproate on Propofol

NCT01170377 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2015-10-21

No results posted yet for this study

Summary

The aim of this study is to evaluate the effect of valproate on the required dose of propofol for sedation in patients with mental retardation.

Conditions

  • Mental Retardation

Sponsors & Collaborators

  • Okayama University

    lead OTHER

Principal Investigators

  • Minako Ishii, D.D.S. · Department of Dental Anesthesiology and Special Care Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-04-30
Primary Completion
2010-08-31
Completion
2010-08-31

Countries

  • Japan

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01170377 on ClinicalTrials.gov