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Effectiveness of Adjunctive Hyaluronic Acid Application in Coronally Advanced Flap in Single Gingival Recession Sites

Effectiveness of Adjunctive Hyaluronic Acid Application in Coronally Advanced Flap in Miller Class I Single Gingival Recession Sites

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03204565
Enrollment
30
Registered
2017-07-02
Start date
2015-09-30
Completion date
2017-04-24
Last updated
2017-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gingival Recession

Keywords

gingival recession, clinical trial(s).

Brief summary

The purpose of this randomized controlled clinical trial (RCT) is to determine the efficacy hyaluronic acid (HA) in combination with the coronally advanced flap (CAF) for the treatment of single gingival recession site. The hypothesis is that HA will result in improved the clinical outcomes and will reduce the pos-operative morbidity

Detailed description

Gingival recession is a common clinical finding in patients with high standards of oral hygiene and can be found in more than 90% of patients. Buccal exposure of roots with aesthetic impairments and dentinal hypersensitivity The ultimate goal of root coverage procedures is the complete coverage of the recession defect with an aesthetic appearance comparable to adjacent healthy soft tissues in combination with physiological probing pocket depths.Several surgical techniques have already provided good results and have been shown to attain root coverage at individual recession sites these different methods.To date, connective tissue grafts (CTG) and enamel matrix derivatives (EMD) in conjunction with a coronally advanced flap (CAF) have been shown to provide the highest probability of obtaining complete root coverage (CRC) in Miller class I and II single gingival recession as compared to CAF alone. Hyaluronic acid (HA) is a major component of the extracellular matrix in almost all tissues. The primary role of HA is to bind water and to permit the transportation of key metabolites and therefore to maintain the structural and homeostatic integrity of these tissues. In vitro and animal studies have demonstrated that hyaluronic acid have many properties that are essential for tissue regeneration and wound healing. However, to the best of our knowledge, there have been limited clinical application studies in the field of root coverage procedures performed and still no consistent published data with longer follow-ups on the usage of HA are available. Therefore, the aim of this randomized controlled clinical trial (RCT) was to evaluate the potential benefit of the adjunctive use of HA in combination with a coronally advanced flap (CAF) and to compare the outcomes with CAF alone, when treating single Miller Class I gingival recessions.

Interventions

coronally advanced flap alone (CAF- control)

DEVICEhyaluronic acid

hyaluronic acid associated to coronally advanced flap (CAF + HA- test)

Sponsors

University of Roma La Sapienza
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age ≥ 18 years * full-mouth plaque score (FMPS) and full-mouth bleeding score (FMBS) \< 15% (measured at four sites per tooth) * presence of at least one buccal recession (depth ≥2 mm) classified as Miller Class I. Only gingival recession sites localized in the anterior area of the maxillary or mandibular arch (central and lateral incisors, canine and first and second premolars) and associated with aesthetic problems and/or dental hypersensitivity were enclosed * gingival recession with at least 1 mm of keratinized tissue (KT) apical to the recession * presence of a clearly identifiable cemento-enamel junction (CEJ), 10) no teeth with prosthetic crown or restoration with the cervical edge in the CEJ area

Exclusion criteria

* systemic diseases or pregnancy * smokers * systemic antibiotic therapy in the last 6 months * active periodontal disease with a sites (probing pocket depth \<4 mm and no bleeding on probing) * history of mucogingival or periodontal surgery at the experimental site

Design outcomes

Primary

MeasureTime frameDescription
Recession reduction (RecRed)baseline and 18 monthsChanges in recession depth between initial and final. Measured in mm

Secondary

MeasureTime frameDescription
Complete root coverage (CRC)18 monthsAssessed as percentage of sites with complete root coverage
Mean root coverage (MRC)18 monthsAssessed as percentage of mean root coverage for each group.
Post-operative morbidity (pain, swelling and discomfort)7 daysWith an evaluation questionnaire. The interviewer assessed patient's pain, swelling and discomfort at 7 days after procedure using visual analogue scale (VAS) ranging from 0 (no pain/swelling/discomfort) to 10 (maximal pain/swelling/discomfort).
Clinical attachment level gain (CAL-Gain)baseline and 18 monthsDifference between CAL initial and final. Measured in mm
Width of keratinized tissue (KT)baseline and 18 monthsChanges in KT between initial and final. Measured in mm
Probing pocket depth (PPD)baseline and 18 monthsChanges in PPD between initial and final. Measured in mm

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026