- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05932017
Comparison of Gingival Flap Procedure Using Conventional Surgical Loupes vs. Videoscope for Visualization
Comparison of Gingival Flap Procedure Using Conventional Surgical Loupes vs. Videoscope for Visualization. A Pilot Study
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 Overview
Status
Detailed Description
It is well known that tartar makes at-home oral hygiene care more difficult. The plaque and bacteria that accumulate on tartar are considered the primary factors contributing to gum disease. Conventional gum surgery is commonly performed using loupes (magnification glasses). The use of a videoscope, a handheld miniature camera, allows for greater visualization during surgery. While the debris on the root surface of teeth is not visible with loupes, it is easily observed when the root surface is visualized with the high magnification of the videoscope. The videoscope allows for up to 40x magnification to visualize underneath the gumline. The use of loupes and the videoscope are methods of visualization that are standard of care at the Texas A&M College of Dentistry.
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 the videoscope in conjunction with loupes during surgery vs. surgery only using loupes. No aspect of this study is investigational, however, bacterial samples will be collected from the patients at multiple time points to assess outcomes. The collection of bacterial samples for research will be conducted through paper points and an oral rinse. These methods are well-established methods of data collection.
Data will be sent to OralDNA labs for analysis. A special contract is required between the school and the company as they will be paid for the services rendered.
Hypothesis: Does the use of the videoscope in conjunction with loupes, as compared to only using loupes for visualization during surgery, have a positive effect (i.e. reduced inflammation and active disease) on the outcomes of gum surgery.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Texas
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Dallas, Texas, United States, 75246
- Texas A&M University School of Dentistry
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Patients receiving routine, pre-diagnosed, standard of care procedures.
Single cohort of patients receiving previously prescribed treatment.
The only variable will be the modality of visualization utilized on each side of the mouth during the surgical procedure.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Probing Depth (in millimeters)
Time Frame: baseline
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The distance from the soft tissue (gingiva or alveolar mucosa) margin to the tip of the periodontal probe during usual periodontal diagnostic probing. The health of the attachment apparatus can affect the measurement. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). The instrument used to measure the probing depth is the periodontal probe. The periodontal is a calibrated probe used to measure the depth and determine the configuration of a periodontal pocket. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). |
baseline
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Clinical Attachment Level (in millimeters)
Time Frame: baseline
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The distance from the cemento-enamel junction to the tip of the periodontal probe during usual periodontal diagnostic probing. The health of the attachment apparatus can affect the measurement. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). The instrument used to measure the clinical attachment level is the periodontal probe. The periodontal is a calibrated probe used to measure the depth and determine the configuration of a periodontal pocket. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). |
baseline
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Bleeding on Probing (yes or no)
Time Frame: baseline
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Bleeding is observed or not observed around each of 6 surfaces for each individual tooth following the gentle probing into the gingiva to obtain the probing depth measurements (see definition of periodontal probing).
Gingival bleeding indicates the presence of inflammation.
Bleeding on probing is a standard of care observation/finding and clinical sign that indicates the presence of inflammation and the progression of periodontal disease.
|
baseline
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Probing Depth (in millimeters)
Time Frame: These will be collected at 3 months post-surgery.
|
The distance from the soft tissue (gingiva or alveolar mucosa) margin to the tip of the periodontal probe during usual periodontal diagnostic probing. The health of the attachment apparatus can affect the measurement. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). The instrument used to measure the probing depth is the periodontal probe. The periodontal is a calibrated probe used to measure the depth and determine the configuration of a periodontal pocket. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). |
These will be collected at 3 months post-surgery.
|
|
Clinical Attachment Level (in millimeters)
Time Frame: These will be collected at 3 months post-surgery.
|
The distance from the cemento-enamel junction to the tip of the periodontal probe during usual periodontal diagnostic probing. The health of the attachment apparatus can affect the measurement. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). The instrument used to measure the clinical attachment level is the periodontal probe. The periodontal is a calibrated probe used to measure the depth and determine the configuration of a periodontal pocket. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). |
These will be collected at 3 months post-surgery.
|
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Bleeding on Probing
Time Frame: These will be collected at 3 months post-surgery.
|
Bleeding is observed or not observed around each of 6 surfaces for each individual tooth following the gentle probing into the gingiva to obtain the probing depth measurements (see definition of periodontal probing).
Gingival bleeding indicates the presence of inflammation.
Bleeding on probing is a standard of care observation/finding and clinical sign that indicates the presence of inflammation and the progression of periodontal disease.
|
These will be collected at 3 months post-surgery.
|
|
Probing Depth (in millimeters)
Time Frame: These will be collected at 6 months post-surgery.
|
The distance from the soft tissue (gingiva or alveolar mucosa) margin to the tip of the periodontal probe during usual periodontal diagnostic probing. The health of the attachment apparatus can affect the measurement. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). The instrument used to measure the probing depth is the periodontal probe. The periodontal is a calibrated probe used to measure the depth and determine the configuration of a periodontal pocket. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). |
These will be collected at 6 months post-surgery.
|
|
Clinical Attachment Level (in millimeters)
Time Frame: These will be collected at 6 months post-surgery.
|
The distance from the cemento-enamel junction to the tip of the periodontal probe during usual periodontal diagnostic probing. The health of the attachment apparatus can affect the measurement. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). The instrument used to measure the clinical attachment level is the periodontal probe. The periodontal is a calibrated probe used to measure the depth and determine the configuration of a periodontal pocket. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). |
These will be collected at 6 months post-surgery.
|
|
Bleeding on Probing
Time Frame: These will be collected at 6 months post-surgery.
|
Bleeding is observed or not observed around each of 6 surfaces for each individual tooth following the gentle probing into the gingiva to obtain the probing depth measurements (see definition of periodontal probing).
Gingival bleeding indicates the presence of inflammation.
Bleeding on probing is a standard of care observation/finding and clinical sign that indicates the presence of inflammation and the progression of periodontal disease.
|
These will be collected at 6 months post-surgery.
|
|
Probing Depths (in millimeters)
Time Frame: These will be collected at 1 year post-surgery.
|
The distance from the soft tissue (gingiva or alveolar mucosa) margin to the tip of the periodontal probe during usual periodontal diagnostic probing. The health of the attachment apparatus can affect the measurement. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). The instrument used to measure the probing depth is the periodontal probe. The periodontal is a calibrated probe used to measure the depth and determine the configuration of a periodontal pocket. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). |
These will be collected at 1 year post-surgery.
|
|
Clinical Attachment Level (in millimeters)
Time Frame: These will be collected at 1 year post-surgery.
|
The distance from the cemento-enamel junction to the tip of the periodontal probe during usual periodontal diagnostic probing. The health of the attachment apparatus can affect the measurement. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). The instrument used to measure the clinical attachment level is the periodontal probe. The periodontal is a calibrated probe used to measure the depth and determine the configuration of a periodontal pocket. (Definition from the American Academy of Periodontology Glossary of Periodontal Terms). |
These will be collected at 1 year post-surgery.
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Bleeding on Probing
Time Frame: These will be collected at 1 year post-surgery.
|
Bleeding is observed or not observed around each of 6 surfaces for each individual tooth following the gentle probing into the gingiva to obtain the probing depth measurements (see definition of periodontal probing).
Gingival bleeding indicates the presence of inflammation.
Bleeding on probing is a standard of care observation/finding and clinical sign that indicates the presence of inflammation and the progression of periodontal disease.
|
These will be collected at 1 year post-surgery.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bacterial Species Identification
Time Frame: These will be collected at the initial visit
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Fluid from just underneath the subject's gums will be collected using a using a commercially available test (paper strip).
The strip will be analyzed for bacteria.
Minimal discomfort is associated with this procedure.
The bacterial sampling is not routinely done in our clinic and considered to be a research only procedure.
The test samples will be analyzed by OralDNA® Labs.
|
These will be collected at the initial visit
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Bacterial Species Identification
Time Frame: These will be collected at 3 months post-surgery.
|
Fluid from just underneath the subject's gums will be collected using a using a commercially available test (paper strip).
The strip will be analyzed for bacteria.
Minimal discomfort is associated with this procedure.
The bacterial sampling is not routinely done in our clinic and considered to be a research only procedure.
The test samples will be analyzed by OralDNA® Labs.
|
These will be collected at 3 months post-surgery.
|
|
Bacterial Species Identification
Time Frame: These will be collected at 6 months post-surgery.
|
Fluid from just underneath the subject's gums will be collected using a using a commercially available test (paper strip).
The strip will be analyzed for bacteria.
Minimal discomfort is associated with this procedure.
The bacterial sampling is not routinely done in our clinic and considered to be a research only procedure.
The test samples will be analyzed by OralDNA® Labs.
|
These will be collected at 6 months post-surgery.
|
|
Bacterial Species Identification
Time Frame: These will be collected at 1 year post-surgery.
|
Fluid from just underneath the subject's gums will be collected using a using a commercially available test (paper strip).
The strip will be analyzed for bacteria.
Minimal discomfort is associated with this procedure.
The bacterial sampling is not routinely done in our clinic and considered to be a research only procedure.
The test samples will be analyzed by OralDNA® Labs.
|
These will be collected at 1 year post-surgery.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Carlos Parra Carrasquer, DDS, Texas A&M University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB2022-1044
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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