Reconstruction of Interdental Papilla Using Hyaluronic Acid

Damascus University

Status: Completed

Conditions: Defected Interdental Papilla

Study type: Observational

Funder types: Other

Identifiers

NCT02119741

UDDS-Perio-02-2014

Details and patient eligibility

About

Objective and background: The aim of this study is to evaluate the clinical outcome of using the hyaluronic acid gel in reconstructing inter-dental papillae at the aesthetic zones in a follow-up period of six months.

Materials and Methods: 30 interdental papilla deficiencies which would meet the the inclusion criteria will be evaluated. After applying local anesthesia, 0.2 ml hyaluronic acid gel will be injected at the affected areas. This procedure will be repeated 3 times for the evaluated areas. Photographs will be taken before injection this material, and at 3 and 6 months following the intervention.

Full description

The presence or absence of the interproximal papilla is essential concern to periodontists, restorative dentists, and to the patients. The loss of papilla can cause cosmetic deformities (black triangles), phonetic problems, and food debris accumulation. Often the loss of papilla is a consequence of periodontal disease because of gingival inflammation, attachment loss and interproximal bone height resorption.

Several reasons also lead to absence of interdental papillae including:

1. Plaque associated lesions, 2) Traumatic oral hygiene procedures, 3) Abnormal tooth shape, 4) Improper contours of the restoration, 5) Spacing between teeth, 6) Loss of teeth.

Enrollment: 30 patients

Sex: All

Ages: 20 to 35 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

The patient should be:

• 20-35 years old.
• Healthy with no systemic diseases.
• Non-smoker and non-alcoholic.
• with good oral hygiene.
• with healthy periodontal tissues.
• suffering from one defected interdental papilla at least.

Defected interdental papilla criteria:

• Class 2 according to Jemt Classification (Jemt 1997).
• The contact points between the teeth should be present.
• There are no restorations or caries in the adjacent teeth.
• The distance between the contact point and the interdental bone crest ≤ 6mm assessed radiographically.

Exclusion criteria

• History of allergic reaction to Hyaluronic acid
• Parafunctional habits.
• Traumatic occlusion.
• The patient under orthodontic treatment.
• Pregnant and lactating women.

Trial design

30 participants in 1 patient group

Affected Interdental Papillae Group

Description:

This is the only group in which the material will be used