Overview
The aim of this study is to evaluate the effect of hyaluronic acid gel in papilla augmentation.
Description
Assessing the clinical efficacy of Hyaluronic acid hydrogel in papilla augmentation: A clinical study.
In Test group, Hyaluronic acid hydrogel will be injected using a syringe into the interdental papillary deficiency site.
In Control group, saline placebo gel will be injected into the interdental papillary deficiency site using a syringe.
Eligibility
Inclusion Criteria:
- Non-smoking patients aged above 18 years.
- Have at least one site with interdental papilla recession in the anterior region (central incisors, lateral incisors and canines) of the maxillary or mandibular jaws.
- Class I or Class II papillary recession.
- The distance from the contact point to alveolar bone crest ≥5mm.
- No active periodontal diseases and good oral hygiene.
Exclusion Criteria:
- spacing or crowding between the teeth to be treated,
- abnormal tooth shape,
- systemic diseases such as diabetes mellitus, hypertension or
- conditions that alter the outcome of periodontal therapy.
- Pregnant and lactating women and
- tobacco users