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Hydroxyapetite Nanoparticles, Tricalcium Phosphate Nanoparticles, and PRF for Treatment of Gingival Recession

O

October 6 University

Status

Completed

Conditions

Periodontitis

Treatments

Other: Nanocrystalline tricalcium phosphate loaded in PRF
Procedure: coronally advanced flap
Other: Nanocrystalline hydroxyapatite loaded in PRF

Study type

Interventional

Funder types

Other

Identifiers

NCT06016894
khafrelsheikh university

Details and patient eligibility

About

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.

Full 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.

Enrollment

20 patients

Sex

All

Ages

20 to 45 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

Nanocrystalline hydroxyapatite
Active Comparator group
Description:
Nanocrystalline hydroxyapatite loaded in PRF+ coronally advanced flap
Treatment:
Procedure: coronally advanced flap
Other: Nanocrystalline hydroxyapatite loaded in PRF
Nanocrystalline tricalcium phosphate (NcTCP)
Active Comparator group
Description:
Nanocrystalline tricalcium phosphate (NcTCP) loaded in PRF+ coronally advanced flap
Treatment:
Other: Nanocrystalline tricalcium phosphate loaded in PRF
Procedure: coronally advanced flap

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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