What this study is
This study is being performed to compare different methods of visualization during routine gum surgery. The gum surgery is standard of care. This study will compare the use of a small camera (videoscope) in conjunction with magnification glasses during surgery vs. surgery only using magnification glasses. Both methods are routinely used and are standard of care methods of visualization. The small camera (videoscope) is a device which allows us to see the area under high magnification and projects live video feed on a computer screen.
The study is a split-mouth design pilot study. The patients are only receiving treatment that was previously diagnosed prior to entering the study. The treatment performed is standard treatment that fits in the routine standard of care. No interventional treatment is being performed. The only difference is the method of visualization/observation by the practitioner used during the surgical procedure. One side of the mouth will be treated with just loupes while the other side of the mouth will be treated with loupes and the videoscope.
Study details
- Official title
- Comparison of Gingival Flap Procedure Using Conventional Surgical Loupes vs. Videoscope for Visualization. A Pilot Study
- Sponsor
- Texas A&M University
- Conditions
- Periodontal Diseases · Periodontal Pocket · Periodontitis · Periodontal Inflammation · Periodontal Attachment Loss · Periodontal Bone Loss · Surgery
- Enrolling
- 20 people
- Starts
- 2023-07-01
- Est. completion
- 2025-03
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers AcceptedYou may qualify if
- Patients that are treatment planned for open flap debridement in two or more quadrants
- Age >18 years old
- Stage III periodontitis diagnosis
- Probing depths ≥5mm with bleeding on probing
You can't join if
- Systemic disease affecting bone metabolism
- Current smokers
- Diabetes
- Pregnant women
- Adults unable to consent
- Prisoners
- Previous or current bisphosphonate use
- Recent joint replacement requiring prophylactic antibiotics
- Teeth that necessitate and undergo osseous recontouring (shaping of the bone) will be excluded
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openTexas A&M University School of Dentistry
Dallas, Texas, United States
Study team
Sponsor
Texas A&M University
Study ID IRB2022-1044
Principal investigator
Carlos Parra Carrasquer, DDS
Texas A&M University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.