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Ultrasonic vs Radiographic Measurement of Gingival Biotype. A Novel Method

Labial Gingival and Osseous Thickness of Upper and Lower Incisors in Thick and Thin Biotypes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03735394
Enrollment
30
Registered
2018-11-08
Start date
2017-04-15
Completion date
2017-09-08
Last updated
2018-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gingival Recession

Keywords

Gingival thickness, gingival biotype, gingival recession, maxilla, mandible

Brief summary

This clinical study consists on taking 2 different records of the upper and lower incisors area : 1) a perpendicular x-ray and 2) an ultrasonic measurement of gingival thickness on the labial plate. Both measurements are used in order to measure gingival and bone thickness. The aim was to verify the reliability of the tissue measurements of an ultrasonic technique compared with the radiographic technique and to verify whether the biotype has correlation between the maxillary and mandibular biotype in the same patient.

Detailed description

The examination of the patients included: * One color photograph of the upper and lower incisors complex with the periodontal probe introduced on the gingival sulcus * Gingival thickness of the most protruded upper and lower incisors was measured with the biometric scanner PIROP. A lip expander was placed and clorhexidine gel was applied on top of the ultrasonic head for better wave conduction. Measurements were taken 10 times at the same point and a mean measurement was obtained. * A tangential radiograph was taken on each patient perpendicular to the axis of the crown of the central upper and lower incisors with a periapical film holding system, and a metal strip (5mm x 1mm x 0,1mm) placed labial to the keratinized gingiva following the inclination of the incisor. A lip expander was used to keep the lips from touching the metal strip. Air was blown over the attached gingiva before placing the metal strip. The metal strip was placed along the long axis of the most protruded lower incisor crown. All patients were evaluated and categorized in one of three possible categories: A1 (7 patients, 23,3%), A2 (12 patients, 40%), and B (11 patients, 36,7%). The patients were assigned into each category by two examiners, according to the visual and clinical aspect of the keratinized gingiva in the lower incisors. Group A1 and A2 both had thin keratinized gingiva and differed in width (group A1 comprised values ≤2mm, and group A2 had width values \>2mm of keratinized gingiva). Group B comprised thick and wide keratinized gingiva. Width of gingiva was measured with a periodontal probe. Thickness of gingiva was assessed by probe transparency, where the examiner determined whether the periodontal probe was visible through the marginal soft tissue. Radiographic measurements Radiographs were scanned at a 1:1 scale. Scanned images were saved in JPEG format. Millimetric measurements were made using the Adobe Photoshop program to a 0.1mm precision. Four measurements were taken on each radiograph: 1. Gingival thickness on the upper incisor 2. Bone thickness on the upper incisor 3. Gingival thickness on the lower incisor 4. Bone thickness on the lower incisor Gingival thickness was measured on the radiographs to compare it with the measurements taken with the biometric scanner. This was a founded and a reliable method to validate the use of the scanner. A master file was created and the data were statistically analyzed using a statistical software package. Size of the sample was obtained with the correlation of lower gingiva and thickness of lower gingiva. The result was 26 calculated with the correlation coefficient 0,587. A 20% tax of follow-up loss was estimated. Intraexaminer reliability was determined using intraclass correlation coefficient (ICC) with a positive confidence interval at 95% (IC 95%). An ICC was used to compare the valid method for group classification between visual and probe transparency methods. The data were subjected to 95% confidence interval for the mean of all variables. The strength of correlation was determined by a P value \<0.05, which was considered statistically significant.

Interventions

DIAGNOSTIC_TESTultrasonic probe

apply the head of the ultrasonic probe on the keratinized tissue of the most protruded upper and lower central incisor in order to measure tissue thickness.

Sponsors

Universitat Internacional de Catalunya
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* aged 18 years or older, * presence of all lower incisors * good periodontal health without bone loss or gingival inflammation * no dental compensations of skeletal malocclusion * crowding of less than 4mm * no history of dental or traumatic lesions in lower incisors

Exclusion criteria

* gingival inflammation * daily smokers * patients taking drugs that causes gingival inflammation

Design outcomes

Primary

MeasureTime frameDescription
compare between maxilla and mandibular biotype measured with the periodontal probe1 dayClassify all patients into one of the three established categories (A1, A2, B) with the aid of a periodontal probe, and compare within the same patient if the biotype of maxilla and mandible is the same or it differs

Secondary

MeasureTime frameDescription
Differences in tissue thickness according to gender1 dayClassify patients in male or female and measure tissue thickness regardless of the biotype measured with both the radiographic technique and ultrasonic device
thickness biotype differences1 dayestablish a possible correlation between maxilla and mandible tissue thickness according to the three possible established categories of biotype measured with radiographic technique and ultrasonic device

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026