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Clinical Trials/RBR-8rvtccf
RBR-8rvtccf
Not yet recruiting
Phase 4

Pain management and clinical characteristics after Gingival Surgery in smokers and non-smokers: randomized controlled trial

niversidade Federal de Pelotas0 sitesJanuary 5, 2024

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Tobacco Use Disorder
Sponsor
niversidade Federal de Pelotas
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 5, 2024
End Date
September 30, 2026
Last Updated
2 years ago
Study Type
Intervention

Investigators

Sponsor
niversidade Federal de Pelotas

Eligibility Criteria

Inclusion Criteria

  • Men and women aged at least 18 years; available to participate in all study phases; with a diagnosis of periodontal health in either intact or reduced periodontium; requiring ACC periodontal surgery with a need for osteotomy of at least 1 mm to restore supracrestal structures (periapical radiographs and/or transperiodontal probing will be used to determine the need for osteotomy in these patients); in the non\-smoker group, only individuals who report never having smoked or having quit smoking for more than five years will be included; in the smoker group, only individuals who report daily consumption of at least ten cigarettes will be included

Exclusion Criteria

  • Individuals requiring crown lengthening for purely aesthetic purposes; those using any type of orthodontic appliance; individuals with soft or hard tissue tumors in the oral cavity; presence of active infectious foci (endodontic abscesses); chronic use of analgesics or anti\-inflammatories for any condition, or use of any analgesics, anti\-inflammatories, or chlorhexidine mouthwashes in the seven days preceding the periodontal surgery; this also includes pregnant or lactating; those who have received local or systemic antimicrobial treatment in the last 90 days; individuals requiring antimicrobial prophylaxis for dental treatment; individuals with a history of allergy to paracetamol, ibuprofen, or dipyrone, including their byproducts; a history of allergy to chlorhexidine, including its byproducts; patients with uncontrolled systemic diseases (such as diabetes); patients on anticoagulants or platelet anti\-aggregants

Outcomes

Primary Outcomes

Not specified

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