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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06016894
Other study ID # khafrelsheikh university
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2000
Est. completion date April 22, 2023

Study information

Verified date August 2023
Source October 6 University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the present study was to compare between nanocrystalline hydroxyapatite and tricalcium phosphate carried on PRP membrane in treatment of Miller's class 1 gingival recession in human.


Description:

gingival recession (GR) is apical movement of the gingival margin beyond the cement-enamel junction. The use of free gingival grafts, sliding pedicle grafts, subepithelial connective tissue grafts, envelope or tunnelling techniques, the use of acellular dermal, connective tissue allografts, guided tissue regeneration, Platelet rich fibrin (PRF), and coronally advanced flap (CAF) are the surgical methods that have been developed to treat gingival recession. For treatments of intrabony defects, a synthetic nanocrystalline hydroxyapatite (NcHA) bone graft has been introduced. Osteoconductivity, bioresorbability, and close contact are benefits of NcHA material. Critical size defects showed quick healing when the NcHA was utilised as a bone graft alternative. NcHA binds to bone and increases osteoblast activity to promote bone regeneration. A promising bone replacement material, tricalcium phosphate (TCP) is known for its strong bioactivity and resorbable qualities. Tricalcium phosphate (TCP) is one of the most popular and effective artificial bone substitutes. It is osteoinductive as well as osteoconductive. These characteristics enable full bone defects regeneration together with its cell-mediated resorption. In this study, we compared between nanocrystalline hydroxyapatite and tricalcium phosphate carried on PRP membrane in treatment of Miller's class 1 gingival recession in human.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 22, 2023
Est. primary completion date September 20, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria: - Patients with good systemic health and no contraindication for periodontal surgery. - Patients who are able to maintain good oral hygiene. - Gingival thickness for the site selected should be =1mm. - The height of keratinized gingiva (HKG) for the site selected should be =1 mm (HKG is the distance between the most apical point of the gingival margin and the mucogingival junction). Exclusion Criteria: - Active infectious diseases (hepatitis, tuberculosis, HIV, etc….). - Medically compromised patients. - Patients taking medications known to cause gingival enlargement. - Pregnant patients and smokers. - Previous mucogingival surgery at the defect. - Restorations or caries in the area to be treated and non vital tooth. - Teeth which are tilted or rotated.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
coronally advanced flap
coronally advanced flap operation
Other:
Nanocrystalline hydroxyapatite loaded in PRF
Nanocrystalline hydroxyapatite loaded in PRF
Nanocrystalline tricalcium phosphate loaded in PRF
Nanocrystalline tricalcium phosphate (NcTCP) loaded in PRF

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
October 6 University

Outcome

Type Measure Description Time frame Safety issue
Primary Recession height measurement recession height 6 months
Primary Recession width measurement of Recession width 6 months
Primary Height of the keratinized tissue measurement of Height of the keratinized tissue 6 months
Primary Percentage of root coverage It is calculated after 1, 3, 6 months as [RH preoperative - RH postoperative]/RH preoperative) x 100%. 6 months
Primary Radiographic assessment measurement of buccal bone gain 6 months
Secondary Probing pocket depth measurement of Probing pocket depth 6 months
Secondary Clinical attachment level measurement of Clinical attachment level 6 months
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