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Efficacy of Clonidine and Propranolol in Dentistry (AAA)

NCT01784250 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2013-02-05

No results posted yet for this study

Summary

The aim of the study is to determine the efficacy of clonidine and propranolol for transient anxiety management and intra and postoperative pain in patients undergoing ambulatory surgery of third molar.

Conditions

Interventions

DRUG

Clonidine

Clonidine 150 mcg tablet single dose, to receive by mouth one hour before surgery

DRUG

Propranolol

Propranolol 40 mg tablet single dose, to receive by mouth one hour before surgery

DRUG

Placebo

Sugar pill manufactured to mimic a drug

Sponsors & Collaborators

  • CES University

    lead OTHER

Principal Investigators

  • Patricia Bermudez, Dentistry · CES University

  • Libia M Rodriguez, Magister · CES University

  • Ana K Tamara, Physician · CES University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2013-04-30
Completion
2013-04-30

Countries

  • Colombia

Study Locations

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Entities

Drugs
Diseases

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 NCT01784250 on ClinicalTrials.gov