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
| Type | Name | Description |
|---|---|---|
| DRUG | 100 mg of Valeriana officinalis L | A single dose of 100 mg of Valeriana officinalis L., 1 hour prior to surgical procedures |
| DRUG | Placebo 100mg | A 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.