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Recruiting Not applicable

Post-Extraction Healing: microRepair vs Chlorhexidine

NCT07555366 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2024-09-01
Last updated
2026-04-29

Condition(s) studied

Endodontic IssuePeriodontal Issues

Investigational drug(s) / intervention(s)

microRepair ABX MousseCHX mouthwash 0.20%

microRepair ABX Mousse: Topical application of the mousse on the surgical wound starting from the day after the extraction. The mousse is specifically formulated to promote healing through microparticles that accelerate tissue repair and an antibacterial complex to prevent localized infections.

CHX mouthwash 0.20%: Application of 0.20% Chlorhexidine liquid mouthwash. Used as a control treatment to evaluate the comparative effectiveness of the test product in reducing plaque, pain, and inflammation while promoting socket healing.

Study summary

This randomized clinical trial evaluates the efficacy of a microRepair ABX mouthwash mousse compared to 0.20% chlorhexidine in promoting wound healing following tooth extraction. The study monitors clinical parameters such as pain, swelling, and healing indices at 1, 7, and 15 days post-surgery. The primary objective is to determine if the microRepair ABX technology enhances tissue regeneration and reduces post-operative complications.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: Age range: Patients between 18 and 75 years of age. Indication for tooth extraction: Specifically for cases involving: * Destructive caries that do not allow for conservative or prosthetic recovery. * Untreatable endodontic and/or periapical lesions. * Advanced periodontal lesions with significant loss of supporting tissue. * Traumatic lesions involving root fractures (vertical or at the middle third). * Malpositioned teeth causing functional alterations. * Roots that cannot be prosthetically recovered or residual roots. Exclusion Criteria: Age: Patients under 18 or over 75 years of age. Systemic Conditions: Presence of immunodepression or immunocompromisation (e.g., HIV infection). Pregnancy and Lactation: Women who are currently pregnant or breastfeeding. Mental Health: Presence of psychiatric disorders. Tobacco Use: Severe smokers, defined as consuming more than 10 cigarettes per day. Substance Abuse: History of alcohol or drug abuse.

Primary outcome measure(s)

  • Plaque Index at the Tooth Extraction Site — From enrollment to the end of treatment at 15 days
    Assessment of the presence or absence of visible bacterial plaque at the tooth extraction site, recorded as a dichotomous variable (Yes/No). The absence of plaque indicates better oral hygiene and a lower risk of postoperative infection.
  • Gingival Condition of the Peri-Alveolar Tissue — From enrollment to the end of treatment at 15 days
    Evaluation of the gingival tissue surrounding the extraction socket based on the presence or absence of clinical signs of inflammation (e.g., redness, edema), recorded as a dichotomous variable (Yes/No). The absence of inflammation indicates healthier gingival tissue.

Trial sites (1)

FacilityCityRegionStatus
Sapienza università di Roma Roma RM Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07555366 on ClinicalTrials.gov ↗ ← All trials in Italy