Efficacy of Clonidine and Propranolol in Dentistry (AAA)

Anxiety Clinical Trial

Official title:

Efficacy of Clonidine and Propranolol Versus Placebo for the Control of Anxiety During Surgical Procedures in Dentistry

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01784250
• Other study ID #: CLON000
• Status: Recruiting
• Phase: Phase 2
• First received: January 23, 2013
• Last updated: February 2, 2013
• Start date: August 2012
• Est. completion date: April 2013

Study information

• Verified date: February 2013
• Source: CES University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Colombia: INVIMA Instituto Nacional de Vigilancia de Medicamentos y Alimentos
• Study type: Interventional

Clinical Trial 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.

Description:

There will be a randomized, triple-blind, placebo-controlled clinical trial with parallel group design to determine the efficacy of the pre medication propranolol and clonidine versus placebo for reducing anxiety during third molar removal surgery. Patients will be assigned to 3 groups of 20 patients each. One group will receive 150 mcg of clonidine, the second group will receive propranolol 40mg, and the control group will receive placebo. The modified dental anxiety scale will be applied before and after surgery in order to evaluate the change in anxiety level, which will be assessed as the primary outcome. The secondary outcomes include the measurement of changes in blood pressure, heart rate and respiratory rate evaluated before, during and after surgery. Additionally, pain will be assessed through numerical pain scale at 3, 6 and 24 hours after surgery. Also, possible side effects will be identified (vomiting, nausea, dry mouth, dizziness and drowsiness). Statistical analysis: qualitative variables will be described by absolute and relative frequencies, and quantitative variables will be described by the mean along with standard deviation or the median with interquartile range depending on the distribution of the data. One-way ANOVA or Kruskal Wallis will be used (depending on the fulfillment of assumptions) in order to compare the quantitative variables amongst the groups. The chi squared test will be used to compare the qualitative variables. The confidence intervals will be estimated at 95% for all effect magnitude measurements calculated.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: April 2013
• Est. primary completion date: April 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 14 Years to 40 Years

Eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Anxiety

Intervention

Drug:
• Clonidine
Clonidine 150 mcg tablet single dose, to receive by mouth one hour before surgery
• Propranolol
Propranolol 40 mg tablet single dose, to receive by mouth one hour before surgery
• Placebo
Sugar pill manufactured to mimic a drug

Locations

Country	Name	City	State
Colombia	Cooperative University	Envigado	Antioquia

Sponsors (1)

Lead Sponsor	Collaborator
CES University

Country where clinical trial is conducted

Colombia, 

References & Publications (7)

Hall DL, Tatakis DN, Walters JD, Rezvan E. Oral clonidine pre-treatment and diazepam/meperidine sedation. J Dent Res. 2006 Sep;85(9):854-8. — View Citation

Herr KA, Spratt K, Mobily PR, Richardson G. Pain intensity assessment in older adults: use of experimental pain to compare psychometric properties and usability of selected pain scales with younger adults. Clin J Pain. 2004 Jul-Aug;20(4):207-19. — View Citation

Humphris GM, Dyer TA, Robinson PG. The modified dental anxiety scale: UK general public population norms in 2008 with further psychometrics and effects of age. BMC Oral Health. 2009 Aug 26;9:20. doi: 10.1186/1472-6831-9-20. — View Citation

Kvale G, Berggren U, Milgrom P. Dental fear in adults: a meta-analysis of behavioral interventions. Community Dent Oral Epidemiol. 2004 Aug;32(4):250-64. — View Citation

Lago-Méndez L, Diniz-Freitas M, Senra-Rivera C, Seoane-Pesqueira G, Gándara-Rey JM, García-García A. Postoperative recovery after removal of a lower third molar: role of trait and dental anxiety. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 Dec;108(6):855-60. doi: 10.1016/j.tripleo.2009.07.021. — View Citation

Liu HH, Milgrom P, Fiset L. Effect of a beta-adrenergic blocking agent on dental anxiety. J Dent Res. 1991 Sep;70(9):1306-8. — View Citation

Ng SK, Leung WK. A community study on the relationship of dental anxiety with oral health status and oral health-related quality of life. Community Dent Oral Epidemiol. 2008 Aug;36(4):347-56. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Frequency of side effects in patients treated with clonidine and propranolol compared with placebo after third molar surgery		24 hours	Yes
Primary	Change from baseline in modified dental anxiety scale(MDAS)and vital signs (blood pressure, heart rate, respiratory rate, oxygen saturation) until four hours post treatment		(plus or minus 4 hours) after surgery	No
Secondary	Changes in Verbal Numerical Rating Scale (VNRS) at three, six, and twenty-four hours post treatment		24 hours	No