The Use Of Specially Designed Probe Versus Cone- Beam Computerized Tomography In The Measurement Of Gingival Thickness: Diagnostic Accuracy Study
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| ClinicalTrials.gov Identifier: NCT03628742 |
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Recruitment Status : Unknown
Verified August 2018 by Deyaa Darwish, Cairo University.
Recruitment status was: Not yet recruiting
First Posted : August 14, 2018
Last Update Posted : August 14, 2018
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Accurate measurement of gingival thickness is crucial for decision making in the field of Periodontology and implant dentistry. Currently implemented techniques for the detection of gingival biotype are of limited reliability. They possess different drawbacks leading to the necessity for the development of a new method to overcome disadvantages of the available techniques.
the rational of this study is to determine the accuracy of a specially designed probe in comparison to cone- beam computerized tomography which is accurate enough as found by Fu et al 2010.
| Condition or disease |
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| Gingival Thickness Gingival Biotype Periodontal Probe |
Show detailed description
| Study Type : | Observational |
| Estimated Enrollment : | 24 participants |
| Observational Model: | Other |
| Time Perspective: | Cross-Sectional |
| Official Title: | The Use Of Specially Designed Probe Versus Cone- Beam Computerized Tomography In The Measurement Of Gingival Thickness: Diagnostic Accuracy Study |
| Estimated Study Start Date : | August 20, 2018 |
| Estimated Primary Completion Date : | December 1, 2018 |
| Estimated Study Completion Date : | May 1, 2019 |
- Special Designed Probe [ Time Frame: finish the trial in 1 years from the clinical trial registration ( May 2019) ]Assessment of the diagnostic accuracy of Specially designed probe in measuring the gingival thickness in millimeter unit
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| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
Inclusion criteria :
- In periodontally healthy individuals.
- Patients with condition indicated for CBCT in upper anterior region
- Patient age 18-50 years.
- Intact maxillary central incisors.
Exclusion criteria:
- Pathological lesion in examined site.
- Any tooth Malalignment in the examined site.
- Patients using drugs which may induce gingival enlargement.
- Pregnant females.
- Any tooth with any metal restoration in the examined site.
| Responsible Party: | Deyaa Darwish, pricipale investigator, Cairo University |
| ClinicalTrials.gov Identifier: | NCT03628742 |
| Other Study ID Numbers: |
cairo univesity |
| First Posted: | August 14, 2018 Key Record Dates |
| Last Update Posted: | August 14, 2018 |
| Last Verified: | August 2018 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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periodontal probe gingival thickness gingival biotype |

