Efficacy of Clonidine and Propranolol in Dentistry (AAA)

• Status: Unknown status
• Trial end date: 2013-04-01
• Target enrollment: 0
• Participant gender: All

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.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: CES University
• Treatments: Clonidine; Propranolol

Criteria

Inclusion Criteria:

• Normotensive patients and pre-hypertension who are undergoing elective surgery for removal of third molars.

• Age range 14 to 40 years

• Patients with dental anxiety above 13 points on the scale (MDAS).

• People who voluntarily agree to participate in the study and sign the informed consent form

Exclusion Criteria:

• Patients receiving any medication for any chronic pathology.

• Patients of African American race, being more likely to have abnormal blood pressure.

• Patients with a history of cardiovascular disease.

• Patients with chronic systemic disease such as diabetes, hyper or hypothyroidism, Addison's syndrome, renal failure, hypertension or liver disease.

• Pregnant or breastfeeding.

• Patients diagnosed with anxiety disorder or depressive disorder