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NCT00970112 Clinical Trial

Dexamethasone and Etoricoxib for Pain Prevention Following Periodontal Surgery

Pain Control Clinical Trial

Official title:
O Uso de Dexametasona e Etoricoxibe Para a prevenção e Controle da Dor pós-operatória após Cirurgia Periodontal

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00970112
Other study ID # 08169/08
Secondary ID 51/2008
Status Completed
Phase Phase 2/Phase 3
First received August 31, 2009
Last updated May 17, 2010
Start date November 2008
Est. completion date March 2010

Study information
Verified date March 2010
Source Universidade Estadual de Ponta Grossa
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate whether preemptive medication with dexamethasone or etoricoxib provides better pain management and control than placebo following periodontal surgery.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date March 2010
Est. primary completion date September 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 55 Years
Eligibility Inclusion Criteria:

- Patients presenting moderate or severe periodontitis after nonsurgical periodontal treatment with clinical signs of inflammation

Exclusion Criteria:

- Pregnant

- Diabetes mellitus

- Heart diseases

- Allergic to components of the medications

- Risk of endocarditis

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Open Flap Debridement
Open flap debridement - access flap + scaling and root planning

Locations
Country Name City State
Brazil UEPG Ponta Grossa Paraná

Sponsors (1)
Lead Sponsor Collaborator
Universidade Estadual de Ponta Grossa

Country where clinical trial is conducted

Brazil, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain hourly for the 8 first hours after surgery 3 times a day on the following 3 days up to 3 days Yes
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