Effect of systemic Corticosteroid use after Maxillary Sinus Lift Surgeries

Not Applicable

• Conditions: Sinus Floor Augmentation; E06.892

• Registration Number: RBR-9ghqkdx
• Lead Sponsor: Faculdade de Odontologia da Universidade Federal do Rio Grande do Sul

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-07-18
• Last Update Posted: 22 August 2023
• Study Completion: 2024-06-01

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Volunteers patients (18 years of age or older); both sexes; patients in need of maxillary sinus lift surgery

Exclusion Criteria

Volunteers with previous chronic or acute pain; volunteers in chronic or acute systemic use (in the 48 hours prior to the procedure) of analgesic, anti-inflammatory and/or muscle relaxant; volunteers with difficulty in understanding instructions (cognitive changes), which impair the application of the scales proposed by the study; illiterate volunteers; volunteers with contraindications for the use of paracetamol associated with codeine; volunteers with contraindication for the use of dexamethasone

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction of postoperative edema after maxillary sinus lift surgery by measuring preoperative facial distances, at 48 hours and at 14 days postoperatively.

Secondary Outcome Measures

Name	Time	Method
Postoperative pain reduction after maxillary sinus lift surgery measured through visual, numerical and verbal assessment scales at 2, 6, 12, 24 and 48 hours postoperatively.