Viewing Study NCT06262945



Ignite Creation Date: 2024-05-06 @ 8:07 PM
Last Modification Date: 2024-10-26 @ 3:21 PM
Study NCT ID: NCT06262945
Status: COMPLETED
Last Update Posted: 2024-02-16
First Post: 2024-02-08

Brief Title: Comperasion the Postoperative Effect of Low Laser Therapy and Platelet Rich Fibrin on Mandibular Third Molar Surgery
Sponsor: Beste Erismen
Organization: Near East University Turkey

Study Overview

Official Title: Comparative Examination of the Postoperative Effects of Low-laser Treatment and Platelet-rich Fibrin Applications After Mandibular Impacted Wisdom Teeth Extraction
Status: COMPLETED
Status Verified Date: 2024-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study was investigate the comparison of postoperative effects of low laser treatment and platelet-rich fibrin application on mandibular impacted third molar tooth extraction The study included a total of 60 patients with impacted mandibular third molar Patients were evaluated in 4 randomly separated groups In group 1 PRF was applied to the tooth socket In group 2 PRF was applied to the tooth socket combined with Low Laser Treatment extraorally to the extraction area for three days within surgery day In group 3 Low Laser Treatment was applied to the extraorally to the extraction area for three days within surgery day In group 4 control group tradional osteomy was made The outcome variables were pain swelling the number of analgesics taken and trismus These variables were also assessed based on first second third and seventh days following the operation All of the 4 groups patients were prescribed an 875125 mg amoxicillinclavulanic acid tablet twice daily for five days
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None