Comparison of Gingival Flap Procedure Using Conventional Surgical Loupes vs. Videoscope for Visualization

December 12, 2024 updated by: Texas A&M University

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

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

Observational

Enrollment (Estimated)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Dallas, Texas, United States, 75246
        • Texas A&M University School of Dentistry

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Patients will be identified at the Texas A&M University dental school clinic.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Probing Depth (in millimeters)
Time Frame: baseline

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
Clinical Attachment Level (in millimeters)
Time Frame: baseline

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
Bleeding on Probing (yes or no)
Time Frame: baseline
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
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.
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.
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
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
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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Carlos Parra Carrasquer, DDS, Texas A&M University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2023

Primary Completion (Estimated)

March 1, 2025

Study Completion (Estimated)

March 1, 2025

Study Registration Dates

First Submitted

March 27, 2023

First Submitted That Met QC Criteria

June 26, 2023

First Posted (Actual)

July 6, 2023

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 12, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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