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Clinical Trials/NCT06761001
NCT06761001
Completed
Not Applicable

Investigation of the Effect of I-PRF Application on Pain in Alveolitis

Eskisehir Osmangazi University1 site in 1 country60 target enrollmentOctober 20, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alveolar Osteitis
Sponsor
Eskisehir Osmangazi University
Enrollment
60
Locations
1
Primary Endpoint
Change in post-operative pain assessed: visual analog (VAS) scale
Status
Completed
Last Updated
last year

Overview

Brief Summary

Literature review showed that there are no studies on the use of i-PRF in alveolitis cases. The aim of this study was to investigate the effect of i-PRF on the treatment of alveolitis. The hypothesis of the study was that i-PRF applied to alveolitis patients would reduce pain.

Detailed Description

The present study will include 60 healthy patients over 18 years of age with alveolitis. 60 patients will be randomly divided into two groups: Control and I-PRF. After irrigation of the sockets, no substance will be applied to the control group, and I-PRF will be applied to the study group. Postoperative pain will be measured on the 3rd and 7th days.

Registry
clinicaltrials.gov
Start Date
October 20, 2024
End Date
February 18, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Eskisehir Osmangazi University
Responsible Party
Principal Investigator
Principal Investigator

Gorkem Tekin

Asst.Prof.

Eskisehir Osmangazi University

Eligibility Criteria

Inclusion Criteria

  • Healthy individuals without systemic disease Patients with complete data and attending their appointments

Exclusion Criteria

  • Patients who smoke Pregnant or breastfeeding female patients with bleeding disorders and diabetics Patients currently or previously using bisphosphonates or receiving radiotherapy to the jaw Patients unable to consent to participate in the study

Outcomes

Primary Outcomes

Change in post-operative pain assessed: visual analog (VAS) scale

Time Frame: postoperative 3rd, and 7th days

VAS measured on a 10cm scale, where 0 represents no pain and 10 represents maximum pain

Study Sites (1)

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