Assessing the Clinical Efficacy of Hyaluronic Acid Hydrogel in Papilla Augmentation: A Clinical Study.

Dr R Viswa Chandra

Status: Enrolling

Conditions: Gingival Destruction

Treatments: Other: Hyaluronic acid gel

Study type: Interventional

Funder types: Other

Identifiers

NCT06447311

SVSInstituteDS4

Details and patient eligibility

About

The aim of this study is to evaluate the effect of hyaluronic acid gel in papilla augmentation.

Full 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.

Enrollment: 24 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Non-smoking patients aged above 18 years.
2. 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.
3. Class I or Class II papillary recession.
4. The distance from the contact point to alveolar bone crest ≥5mm.
5. No active periodontal diseases and good oral hygiene.

Exclusion criteria

1. spacing or crowding between the teeth to be treated,
2. abnormal tooth shape,
3. systemic diseases such as diabetes mellitus, hypertension or
4. conditions that alter the outcome of periodontal therapy.
5. Pregnant and lactating women and
6. tobacco users

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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24 participants in 2 patient groups, including a placebo group

Test group

Experimental group

Description:

In Test group, the prepared Hyaluronic acid gel will be injected using a syringe into the defect site.

Treatment:

Other: Hyaluronic acid gel

Control group

Placebo Comparator group

Description:

In Control group, saline placebo gel will be injected into the defect site using a syringe.

Treatment:

Other: Hyaluronic acid gel