Effect of Premedication on Success of Inferior Alveolar Nerve Block Injection
NCT02601911 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2016-09-20
Summary
The aim of this study is effect of premedication on success of inferior alveolar nerve block injection. Sixty healthy adult volunteers including criteria, are participating. The patients will be divided into 3 groups and will be randomly given one of premedications including 1) 10 mg Ketorolac, 2) 10 mg Ketorolac plus 1000mg Acetaminophen, and 3)Placebo, 45 minutes before applying the injection. All patients will receive standard Inferior Alveolar Nerve Block injection . Patients with no lip numbness and positive responses to cold and electric pulp tests would be excluded from the study. Endodontic access preparation will be initiated 15 minutes after Inferior Alveolar Nerve Block injection. Pain during treatment will be recorded using a Heft parker Visual Analog Scale(VAS). Success will be considered as no or mild pain (VAS≤54) during caries/dentin removal, access cavity preparation and working lengths measurements. Data will be analysed using Mann-U-Whitney and Kruskal-wallis tests.
Conditions
- Irreversible Pulpitis
Interventions
- DRUG
-
Ketorolac Tromethamine
10 mg Ketorolac tromethamine is applied 45 minutes before the injection.
- DRUG
-
10 mg Ketorolac tromethamine/ 1000mg Acetaminophen application before injection.
- OTHER
-
Placebo
This group receive the caplet including placebo 45 minutes before the injection.
Sponsors & Collaborators
-
Azad University of Medical Sciences
lead OTHER
Principal Investigators
-
Nahid Mohammadzadeh Akhlaghi, DDS, MDS · Associate Professor
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2015-09-30
- Primary Completion
- 2016-05-31
- Completion
- 2016-06-30
Countries
- Iran
Study Locations
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