The Use of a Non-Incised Minimally Invasive Flap Procedure in Conjunction With Emdogain® MI Compared to Traditional SRCP

Not Applicable

Recruiting

• Conditions: Periodontitis; Attachment Loss, Periodontal

• Registration Number: NCT05964699
• Lead Sponsor: Texas A&M University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-6-26
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 32

Inclusion Criteria

Inclusion Criteria:<br><br>To participate in this study, you must present:<br><br> - Generalized gum disease with isolated pocket depths of 5 mm to less than 7 mm on<br> bicuspid and cuspid teeth.<br><br> - At least 2 mm of attachment loss.<br><br> - Need to have two similar teeth meeting the criteria for isolated pockets on two<br> other quadrants of the mouth.<br><br> - Need to be between 30 and 75 years of age.<br><br> - Be in good health.<br><br> - Smoke less than 10 cigarettes or equivalent per day.<br><br> - No antibiotics for the past 90 days.<br><br> - Not be taking medications that are known to inhibit or slow healing.<br><br>Exclusion Criteria:<br><br>You are not eligible if:<br><br> - You are pregnant.<br><br> - You are breast feeding.<br><br> - Received gum treatment in the last 6 months.<br><br> - Smoke more than ten cigarettes per day.<br><br> - You have any serious medical conditions.

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Attachment level change.;Probing depth change.;Gingival margin level / recession change.;Bleeding on probing change.;Biofilm presence change.

Secondary Outcome Measures

Name	Time	Method
Time necessary to perform the test procedures;VAS pain scale 24 hours after appointment.;VAS pain scale 1 week after appointment.