Viewing Study NCT04811144



Ignite Creation Date: 2024-05-06 @ 3:56 PM
Last Modification Date: 2024-10-26 @ 2:00 PM
Study NCT ID: NCT04811144
Status: COMPLETED
Last Update Posted: 2021-03-23
First Post: 2021-03-22

Brief Title: Clinical Application of ErYAG Dental Laser System
Sponsor: Kaohsiung Medical University Chung-Ho Memorial Hospital
Organization: Kaohsiung Medical University Chung-Ho Memorial Hospital

Study Overview

Official Title: Clinical Application of ErYAG Dental Laser System
Status: COMPLETED
Status Verified Date: 2021-03
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 study aim was to evaluate the effectiveness of ErYAG dental laser treatment modality for cavity sensitive teeth abnormal frenum attachment and peri-implantitis
Detailed Description: There are four indications will be included in this plan They are Cavity Sensitive Teeth Abnormal Frenum Attachment and Peri-implantitis Each indication has different procedures which are listed as below

Cavity history records affected range check X-rayphoto treatment pain index check return visit check after two weeks Sensitive Teeth history records sensitive check X-rayphoto treatment pain index and effectiveness check return visit check after two weeks Abnormal Frenum Attachment history records abnormal position check photo cutting pain index check return visit check after three five and seven days Peri-implantitis History records measure periodontal pocket depth anaerobes collect X-ray photo CT treatment pain index check return visit check after one week two weeks four weeks and three months six months check the effectiveness and collect anaerobes during every return visit In the last return visit X-ray and CT would be included

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