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Not yet recruitingNCT07529340Updated Apr 20, 2026

Study of Hyaluronic Acid Used With Gum Surgery to Treat Gum Recession in Adults

An interventional study of Coronally Advanced Flap with Connective Tissue Graft and Cross-linked Hyaluronic Acid Gel in Gingival Recession, Mucogingival Surgery, sponsored by Universidade do Porto. Not yet recruiting at 1 site in Portugal. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-04-20.

Sponsored by Universidade do Porto · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Gingival recession is a common condition in which the gum tissue recedes, exposing the root surface of the tooth. This can lead to tooth sensitivity, higher risk of root decay, and aesthetic concerns. A commonly used surgical treatment is the coronally advanced flap combined with a connective tissue graft (CAF + SCTG), which aims to cover the exposed root and improve gum health.

Hyaluronic acid (HA) is a naturally occurring substance in the body that plays an important role in wound healing. It may help improve tissue repair, reduce inflammation, and enhance healing after surgery.

This study aims to evaluate whether the use of hyaluronic acid (hyaDENT BG®) in addition to standard surgical treatment improves clinical outcomes in patients with gingival recession. Participants will be randomly assigned to receive either standard treatment alone or standard treatment with hyaluronic acid.

The main outcome is the proportion of sites with complete root coverage after 12 months. Additional outcomes include healing, gum tissue improvement, patient-reported pain and discomfort, and aesthetic results.

The study also includes a laboratory component to investigate how hyaluronic acid affects cells involved in gum healing.

Read the detailed description

Gingival recession (GR) is a common mucogingival condition characterized by apical displacement of the gingival margin beyond the cemento-enamel junction, leading to root exposure, dentin hypersensitivity, increased risk of root caries, and aesthetic impairment. The coronally advanced flap combined with a subepithelial connective tissue graft (CAF + SCTG) is considered the gold standard for the treatment of single gingival recession defects, providing predictable root coverage and long-term stability. However, postoperative morbidity, donor-site discomfort, and incomplete root coverage may still occur.

Hyaluronic acid (HA) is a key component of the extracellular matrix with biological properties that promote wound healing, including stimulation of angiogenesis, cell migration, proliferation, and modulation of inflammatory responses. Cross-linked HA formulations exhibit prolonged bioactivity and may enhance soft tissue healing and regeneration in periodontal surgery.

This study is a prospective, randomized, controlled, post-market clinical follow-up (PMCF) trial designed to evaluate the clinical effectiveness and safety of adjunctive cross-linked hyaluronic acid (hyaDENT BG®) in combination with CAF + SCTG for the treatment of single RT1 and RT2 gingival recession defects. A total of 34 patients will be enrolled and randomly allocated in a 1:1 ratio to either the test group (CAF + SCTG with adjunctive HA) or the control group (CAF + SCTG alone). Randomization will be stratified by recession type (RT1 vs RT2), and outcome assessors will be blinded to treatment allocation.

The primary endpoint is complete root coverage (CRC) at 12 months, defined as recession depth equal to 0 mm relative to the cemento-enamel junction. Secondary endpoints include mean root coverage, recession reduction, clinical attachment level gain, probing depth reduction, keratinized tissue gain, early wound healing (Early Wound Healing Score), patient-reported outcomes (pain, discomfort, and oral health-related quality of life), and aesthetic outcomes assessed using the Root Coverage Esthetic Score (RES).

Clinical assessments will be performed at baseline and at predefined follow-up visits up to 12 months post-surgery using standardized protocols and calibrated examiners. Patient-reported outcomes will be collected using validated instruments, including visual analog scales (VAS) and the OHIP-14 questionnaire.

In parallel, an in vitro component will be conducted using primary human gingival fibroblasts isolated from connective tissue grafts obtained during surgery. These cells will be used to evaluate the effects of HA on cell viability, proliferation, migration, gene expression related to wound healing and inflammation, and activation of intracellular signaling pathways.

This combined clinical and translational approach aims to provide comprehensive evidence on both the clinical performance and biological mechanisms of action of hyaluronic acid in periodontal plastic surgery.

02

Conditions studied

  • Gingival Recession, Mucogingival Surgery

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Keywords

  • Gingival recession
  • Coronally advanced flap
  • Connective tissue graft
  • Hyaluronic acid
  • Mucogingival surgery
03

In context

Gingival Recession

402 studies on the registry are indexed under Gingival Recession; 98 are open to participants now.

This study's planned enrollment of 34 is above the median of 30 across 368 interventional studies indexed under Gingival Recession.

Browse Gingival Recession studies →

Lead sponsor

Universidade do Porto is the lead sponsor of 170 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • - Age ≥ 18 years, in good general health (ASA I or II)
  • Presence of a single gingival recession defect classified as RT1 or RT2
  • Recession depth ≥ 2 mm with identifiable cemento-enamel junction (CEJ)
  • Presence of at least 1 mm of keratinized tissue at the defect site
  • No active periodontal disease (probing depth ≤ 4 mm and no bleeding on probing at the selected tooth)
  • Full-Mouth Plaque Score (FMPS ≤ 20%) and Full-Mouth Bleeding Score (FMBS ≤ 20%)
  • Vital tooth without caries, cervical lesions, or defective restorations
  • Good oral hygiene and motivation to maintain plaque control
  • Ability and willingness to comply with study procedures
  • Signed informed consent

Exclusion criteria

Exclusion Criteria:

  • Uncontrolled systemic diseases (e.g., uncontrolled diabetes, severe cardiovascular disease, immunodeficiency)
  • Pregnant or breastfeeding women
  • Autoimmune diseases or immunosuppressive therapy
  • Known hypersensitivity to hyaluronic acid
  • Heavy smokers (>10 cigarettes/day) or recent tobacco use
  • Active periodontal disease at the study site
  • Caries, root fractures, endodontic lesions, or defective restorations at the study tooth
  • Previous mucogingival surgery at the study site
  • Recent use of antibiotics, corticosteroids, or anti-inflammatory drugs
  • Coagulation disorders or anticoagulant therapy contraindicating surgery
  • Hormonal disorders affecting wound healing
  • Acute oral infections
  • Any condition that may interfere with study participation or follow-up
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
34 participants (estimated)

Study arms

  • Experimental
    CAF + SCTG + Hyaluronic Acid

    Participants undergo coronally advanced flap (CAF) surgery combined with a subepithelial connective tissue graft (SCTG) with adjunctive application of cross-linked hyaluronic acid (hyaDENT BG®). The graft is immersed in hyaluronic acid prior to placement, and the gel is applied to the recipient site before flap closure.

    Procedure: Coronally Advanced Flap with Connective Tissue Graft · Device: Cross-linked Hyaluronic Acid Gel

  • Active comparator
    CAF + SCTG

    Participants undergo coronally advanced flap (CAF) surgery combined with a subepithelial connective tissue graft (SCTG) without adjunctive hyaluronic acid. The graft is handled under standard conditions and hydrated with sterile saline prior to placement.

    Procedure: Coronally Advanced Flap with Connective Tissue Graft

Interventions

  • ProcedureCoronally Advanced Flap with Connective Tissue Graft

    Standard periodontal plastic surgery procedure for root coverage involving coronally advanced flap (CAF) combined with a subepithelial connective tissue graft (SCTG). The technique aims to cover exposed root surfaces and improve soft tissue thickness and stability.

    Also known as: CAF + SCTG

  • DeviceCross-linked Hyaluronic Acid Gel

    Application of cross-linked hyaluronic acid gel (hyaDENT BG®) as an adjunct to periodontal surgery. The gel is applied to the recipient site and used to immerse the connective tissue graft prior to placement, aiming to enhance soft tissue healing, promote cell proliferation and angiogenesis, and improve clinical outcomes.

    Also known as: hyaDENT BG®

06

What researchers measure

Primary outcomes

  1. Complete Root Coverage (CRC)

    Proportion of treated sites achieving complete root coverage, defined as recession depth equal to 0 mm relative to the cemento-enamel junction, assessed using a calibrated periodontal probe by a blinded examiner.

    Time frame: 12 months

Secondary outcomes

  1. Mean Root Coverage (MRC)

    Percentage of root coverage achieved relative to baseline recession depth at the treated site.

    Time frame: 12 months

  2. Recession Reduction (RecRed)

    Change in gingival recession depth (mm) from baseline to follow-up, measured using a calibrated periodontal probe.

    Time frame: 12 months

  3. Clinical Attachment Level (CAL) Gain

    Change in clinical attachment level (mm) from baseline to 12 months, measured using a periodontal probe.

    Time frame: 12 months

  4. Probing Depth (PD) Reduction

    Reduction in probing depth (mm) from baseline to 12 months, measured using a periodontal probe.

    Time frame: 12 months

  5. Keratinized Tissue Width (KT) Gain

    Increase in the width of keratinized gingiva (mm) from baseline to follow-up.

    Time frame: 12 months

  6. Early Wound Healing Score (EHS)

    Assessment of early soft tissue healing using the Early Wound Healing Score at predefined postoperative time points.

    Time frame: 3 days, 14 days, and 6 weeks

  7. Postoperative Pain and Discomfort (VAS)

    Patient-reported pain and discomfort assessed using a visual analog scale (VAS).

    Time frame: 3 days, 14 days, and 6 weeks

  8. Oral Health-Related Quality of Life (OHIP-14)

    Patient-reported oral health-related quality of life measured using the OHIP-14 questionnaire.

    Time frame: 3 days, 14 days, and 6 weeks

  9. Root Coverage Esthetic Score (RES)

    Esthetic outcome assessed using the Root Coverage Esthetic Score based on standardized clinical photographs.

    Time frame: 12 months

  10. Surgical and Postoperative Complications

    Incidence of intraoperative and postoperative complications, including flap dehiscence, infection, or graft necrosis.

    Time frame: up to 12 months

07

Study locations

1 site
  • CEPI - Clinical Center for Periodontology and Implantology
    Porto, Porto District 4350-110, Portugal
08

References and documents

Publications

  • Guldener K, Lanzrein C, Eliezer M, Katsaros C, Stahli A, Sculean A. Treatment of single mandibular recessions with the modified coronally advanced tunnel or laterally closed tunnel, hyaluronic acid, and subepithelial connective tissue graft: a report of 12 cases. Quintessence Int. 2020;51(6):456-463. doi: 10.3290/j.qi.a44492. PubMed 32368762 ↗
  • Asparuhova MB, Kiryak D, Eliezer M, Mihov D, Sculean A. Activity of two hyaluronan preparations on primary human oral fibroblasts. J Periodontal Res. 2019 Feb;54(1):33-45. doi: 10.1111/jre.12602. Epub 2018 Sep 27. PubMed 30264516 ↗
  • Pilloni A, Schmidlin PR, Sahrmann P, Sculean A, Rojas MA. Effectiveness of adjunctive hyaluronic acid application in coronally advanced flap in Miller class I single gingival recession sites: a randomized controlled clinical trial. Clin Oral Investig. 2019 Mar;23(3):1133-1141. doi: 10.1007/s00784-018-2537-4. Epub 2018 Jun 30. PubMed 29961138 ↗

Study documents

  • Study protocol · Mar 2, 2026

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Undecided — No final decision has been made regarding individual participant data sharing. Data sharing will be considered in accordance with applicable regulations and institutional policies.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07529340
Lead sponsor
Universidade do Porto
Collaborators
Regedent AG, Zürich
Responsible party
Sponsor
First posted
Apr 14, 2026
Start date
May 2026 (estimated)
Primary completion
Sep 2027 (estimated)
Completion
Sep 2027 (estimated)
Last update
Apr 20, 2026

Study contacts

Marta M Abreu-Costa
Contact
martacostaa11@gmail.com
+351911834256

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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