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Clinical Trial Summary

GlaxoSmithKline will be conducting this trial to compare analgesics efficacy of paracetamol 1000mg vs 500mg . The post-surgical dental pain model will be used to evaluate the analgesic efficacy of paracetamol. Each subject will be enrolled in the study for up to six weeks. The duration of the entire study will be approximately 16 weeks. Each subject will have to come to the clinic for three visits (Screening, Treatment and Follow up visits).


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01082081
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 4
Start date October 2009
Completion date March 2010

See also
  Status Clinical Trial Phase
Terminated NCT01512160 - Efficacy Of Pf-04531083 In Treating Post-Surgical Dental Pain Phase 2
Completed NCT01075243 - Post-operative Dental Pain Study Comparing Two Different Dosage of Analgesic Efficacy Phase 4