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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04617301
Other study ID # 2020/98
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 22, 2020
Est. completion date October 21, 2020

Study information

Verified date October 2020
Source Recep Tayyip Erdogan University Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

More accurate management of resorption can be achieved thanks to the three-dimensions volumetric and linear analysis, and the axial classification presented in this study.


Description:

The aim of this study was to investigate the volumetric and linear analysis, and to present the axial classification of root resorptions using cone beam computed tomography (CBCT). A total of 43 teeth of external cervical resorption (ECR) (n=27), external replacement resorption (ERR) (n=4) and internal root resorption (IRR) (n=12) were identified from 34 patients. The volume of resorption and total tooth, the widest lengths of these resorptions, and the amount of thinnest dentin thickness around them were measured and compared according to age and sex. Additionally, the eight regional axial classification was performed and the percentages in these regions were evaluated. Significance was set at p=0.05 for statistical analysis. More accurate management of resorption can be achieved thanks to the three-dimensions volumetric and linear analysis, and the axial classification presented in this study.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date October 21, 2020
Est. primary completion date August 10, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 71 Years
Eligibility Inclusion Criteria: - Cases of resorption that had CBCT images Exclusion Criteria: - those presenting pathologic lesions, congenital/developmental anomalies or teeth with root canal filling - those whose CBCT scans failed to present satisfactory quality. - Additionally, SR, TAP, and EIR cases were excluded because their true dimensions could not be completely determined before resorption.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Recep Tayyip Erdogan University Training and Research Hospital Rize

Sponsors (1)

Lead Sponsor Collaborator
Recep Tayyip Erdogan University Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Heithersay GS. Clinical, radiologic, and histopathologic features of invasive cervical resorption. Quintessence Int. 1999 Jan;30(1):27-37. — View Citation

Patel S, Dawood A, Wilson R, Horner K, Mannocci F. The detection and management of root resorption lesions using intraoral radiography and cone beam computed tomography - an in vivo investigation. Int Endod J. 2009 Sep;42(9):831-8. doi: 10.1111/j.1365-2591.2009.01592.x. Epub 2009 Jul 14. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Volume of total tooth and resorbed area The total volume and the resorption volume were measured with used 3D semi-automatic segmentation program (ITK-SNAP 2.4) for three months from the beginning of the study
Primary Measurement widest mesio-distal length, bucco-lingual length and corono-apical length of the resorbed lesion Linear measurement were measured with used Planmeca ProMax 3D Classic (Planmeca Promax 3D; Planmeca Oy; Helsinki, Finland) for three months from the beginning of the study
Primary Linear measurements for thinnest dentin (buccal, distal, mesial and lingual/ palatinal) and resorbed area (mesio-distal length and bucco-lingual length) were made on axial sections Linear measurement were measured with used Planmeca ProMax 3D Classic (Planmeca Promax 3D; Planmeca Oy; Helsinki, Finland) for three months from the beginning of the study
Primary The corono-apical length was measured on sagittal sections where the tooth axis was perpendicular to the ground plane. Linear measurement were measured with used Planmeca ProMax 3D Classic (Planmeca Promax 3D; Planmeca Oy; Helsinki, Finland) for three months from the beginning of the study
Primary the axial section of the tooth was divided into eight parts and regional settlement classification was performed Segmentation were made with used Planmeca ProMax 3D Classic (Planmeca Promax 3D; Planmeca Oy; Helsinki, Finland) for three months from the beginning of the study
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