Clinical Trials Directory

Trials / Completed

CompletedNCT01612130

Valerian for Conscious Sedation in Patients Submitted to Impacted Lower Third Molars Surgery

Valeriana Officinalis L. for Conscious Sedation in Patients Submitted to Impacted Lower Third Molars Surgery: A Randomized, Double-Blind, Placebo-Controlled Crossover Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Federal University of the Valleys of Jequitinhonha and Mucuri · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

The aim of the present study was to evaluate the efficacy of Valeriana officinalis L. 100 mg in single oral doses one hour preoperative as conscious sedation during the impacted lower third molar surgery.

Detailed description

Evaluate the efficacy of Valeriana officinalis L. (Valerian) for control of anxiety during third molar surgery. Study design: A single oral dose of either valerian (100 mg) or placebo was randomly administered one hour before each surgical procedure to 20 volunteers between 17 and 31 years of age. Anxiety level was assessed through questionnaires, physiological parameters (blood pressure and heart rate) and the observation of signs.

Conditions

Interventions

TypeNameDescription
DRUG100 mg of Valeriana officinalis LA single dose of 100 mg of Valeriana officinalis L., 1 hour prior to surgical procedures
DRUGPlacebo 100mgA single dose of 100 mg of placebo orally, 1 hour prior to surgical procedures

Timeline

Start date
2003-03-01
Primary completion
2003-08-01
Completion
2003-08-01
First posted
2012-06-05
Last updated
2012-06-06

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01612130. Inclusion in this directory is not an endorsement.