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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-20

Study Completion Date

2025-02-18

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Alveolar Osteitis Pain Dry Socket

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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I-PRF

I-PRF Application

Group Type EXPERIMENTAL

I-PRF

Intervention Type DEVICE

After local anesthesia is injected, alveolar curettage is performed and the socket is irrigated with saline solution. I-PRF is given to patients in the experimental group.

Standard treatment

standard treatment

Group Type ACTIVE_COMPARATOR

Control

Intervention Type OTHER

After local anesthesia is injected, alveolar curettage is performed and the socket is irrigated with saline solution.

Interventions

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I-PRF

After local anesthesia is injected, alveolar curettage is performed and the socket is irrigated with saline solution. I-PRF is given to patients in the experimental group.

Intervention Type DEVICE

Control

After local anesthesia is injected, alveolar curettage is performed and the socket is irrigated with saline solution.

Intervention Type OTHER

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes