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Clinical Trials/RBR-4ht99zx
RBR-4ht99zx
Active, not recruiting
Phase 2

Evaluation of the preemptive and preventive use of coadministration of Ibuprofen l-arginine and Dexamethasone on postoperative inflammatory markers, quality of life, sleep quality and pain catastrophizing in lower third molar surgeries: a randomized, split-mouth, factorial, controlled clinical trial

niversidade Federal do Ceará0 sitesOctober 13, 2023

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Anomalies of tooth position
Sponsor
niversidade Federal do Ceará
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 13, 2023
End Date
November 30, 2023
Last Updated
2 years ago
Study Type
Intervention

Investigators

Sponsor
niversidade Federal do Ceará

Eligibility Criteria

Inclusion Criteria

  • Healthy individuals of both sexes; aged between 18\-35 years; in need of removal of the two lower third molars; will be invited to participate in this study. In addition to these, the following inclusion criteria will also be adopted: semi\-erupted or non\-erupted mandibular third molars; third molars that present, on panoramic radiography, similar patterns of root formation, position and degree of impaction when comparing the right and left sides of each volunteer

Exclusion Criteria

  • Volunteers who meet at least one of the following criteria will be excluded: smokers; pregnant or lactating women; users of medications that interact with the drugs used in this study; carriers of orthodontic bands in mandibular second molars; confirmed history of allergy to NSAIDs or corticoids; signs of any preoperative inflammatory or infectious condition; systemic diseases; neurological disorders. In addition, the volunteer who has used any NSAID or corticoid within a period of up to 21 days before the surgical procedure will also be excluded from the research due to the possibility of a residual effect of the drug eventually used, which may influence the outcomes of the present study

Outcomes

Primary Outcomes

Not specified

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