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Clinical Trials/NCT07339605
NCT07339605
Recruiting
Not Applicable

Clinical and Radiographic Outcomes After Flapless Approach of Intrabony Defects With the Application of Enamel Matrix Derivative Versus Hyaluronic Acid: A Randomized Controlled Clinical Trial

University of Valencia1 site in 1 country60 target enrollmentStarted: October 26, 2024Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
60
Locations
1
Primary Endpoint
Radiographic bone fill

Overview

Brief Summary

The goal of this clinical trial is to radiographically assess the effectiveness of minimally invasive non-surgical technique (MINST) combined with local administration of sodium hypochlorite gel (Perisolv®) and 1.6% cross-linked hyaluronic acid (HA, Hyadent BG®) compared to a neutral formulation of EDTA (Prefgel®) and enamel matrix derivative (EMD, Emdogain® FL) in periodontal regeneration. The main questions it aims to answer are:

  • ¿Does the combination of MINST with the local administration of sodium hypochlorite gel and 1.6% cross-linked hyaluronic acid show a potential for periodontal regeneration similar to evaluating clinical and radiographic variables compared to a neutral formulation of EDTA and enamel matrix derivative?
  • ¿What is the patient perception and satisfaction with the received treatment?

Researchers will compare A (MINST with Perisolv® + Hyadent BG®), B (MINST with PrefGel® + Emdogain® FL) and C(MINST without any bioactive product).

The sample will be distributed according to the following treatments:

  • Experimental group: Scaling and root planing (SRP), MINST with Perisolv® + Hyadent BG®.
  • Active comparator group: SRP, MINST with PrefGel® + Emdogain® FL.
  • Control group: SRP, MINST without any bioactive product.

Patients will be screened by a first visit in which they will be assigned their periodontal status. If they meet the eligibility criteria, they will be treated according to the EFP clinical guideline for periodontitis treatment: step I and step II.If the periodontal defect persists at the 12-week re-evaluation, patients will be randomised to treatment A, B or C.

After the intervention, all participants will be checked weekly for the first 6 weeks to remove accumulated plaque, and every 3 months for 1 year. Periodontal parameters will be re-evaluated 6 and 12 months after periodontal regenerative intervention.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Periodontitis stage III or IV, grade A or B (Tonetti et al., 2017): attachment loss ≥ 5mm, radiographic bone loss extending to to the middle third and beyond, tooth loss ≥4 due to periodontitis, probing depth (PD) ≥ 6mm.
  • Older adults ≥ 18 years. The number per sex shall be balanced.
  • Plaque index (PI) \< 1 following initial periodontal therapy and hygiene instructions.
  • Bleeding on probing (BoP) ≤ 10%.
  • Only patients with optimal compliance, assessed during etiological therapy, will be selected.
  • At least a 2-3 wall interproximal bone defect with a radiographically moderate or deep intrabony defect (≥3mm), PD≥ 6mm using a Williams probe on uniradicular teeth or mandibular molars without furcation involvement after non-surgical periodontal treatment.
  • Vital teeth or teeth with well-performed root canal treatment.
  • Absence of caries, prosthetic restoration or periapical infection in the tooth to be regenerated.
  • Absence of systemic pathology.
  • Negative history of pregnancy.

Exclusion Criteria

  • The participant is pregnant, breastfeeding or plans to become pregnant in the next 6 months.
  • Smoking ≥10 cigarettes/day.
  • Daily alcohol intake \> 4U.
  • Chronic illness or reduced mental capacity that may influence compliance with the protocol.
  • Medications or drugs that alter the patient's healing or with concomitant oral manifestations that, in the opinion of the investigator, could interfere with the assessment of safety or efficacy.
  • Systemic diseases that may influence treatment such as diabetes mellitus or rheumatoid disease.
  • Allergies to drug compounds.
  • Antibiotic intake 3 months prior to the start of the study or systemic condition requiring antibiotic coverage at the time of periodontal treatment.
  • Periodontal treatment 6 months prior to the start of the study.

Arms & Interventions

(MINST + NaOCl) + HA

Experimental

Intervention: Flapless instrumentation of the defect following MINST in conjuction with NaOCl and hyaluronic acid application (Procedure)

(MINST + EDTA) + EMD

Active Comparator

Intervention: Flapless instrumentation of the defect following MINST, root conditioning with EDTA and EMD application (Procedure)

MINST

Sham Comparator

Intervention: Flapless instrumentation of the defect and product application simulation (Procedure)

Outcomes

Primary Outcomes

Radiographic bone fill

Time Frame: Baseline, 6 and 12 months.

Depth of the intraosseous defect (B - D); and following the healing period (X - C). Bone fill (BF) will be calculated by subtracting the (X - C) measurement recorded at the 6-month and 12-month postoperative review from the depth recorded before the regenerative intervention (B - D).

Secondary Outcomes

  • Gingival recession(Baseline, 6 and 12 months.)
  • Clinical attachment level (CAL) gain(Baseline, 6 and 12 months.)
  • Probing pocket depth (PD)(Baseline,6 and 12 months.)
  • Bleeding on probing(Baseline, 6 and 12 months.)
  • Plaque index(Baseline, 6 and 12 months.)
  • Chair time(During procedure)
  • Patient satisfaction and perception(1 week after baseline (regenerative intervention))
  • Patient satisfaction and perception(6 months after baseline (regenerative intervention))
  • Patient satisfaction and perception(12 months after baseline (regenerative intervention))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Andres Lopez Roldan

Assistant Professor with PhD

University of Valencia

Study Sites (1)

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