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Clinical Trials in Italy / NCT05073952
Recruiting Not applicable

Keratized Mucosa in CG Implant Placement: CTG vs Flapless

NCT05073952 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2021-10-18
Last updated
2021-12-03

Condition(s) studied

Variation of Keratinized Mucosa After Implant Surgery

Investigational drug(s) / intervention(s)

Connective tissue graftFlapless

Connective tissue graft: Implants will be placed with a flap and a connective tissue graft.

Flapless: Implants will be placed with a flapless approach

Study summary

The present study will evaluate the difference in terms of keratinazed mucosa (KM) in computer guided implant placement with immediate loading, comparing a flapless approach to flap surgery with connective tissue graft.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Age 18+ * Patients with partial edentulism in the posterior region (4-7) upper or lower for at least 3 months * Patient whose tomographic examination shows adequate bone volumes for computer guided placement of a standard diameter implant (\> 3.5 mm) without the need for bone regeneration procedures * Patients who have accepted informed consent and participation in the study * Patients who do not have exclusion criteria Eclusion Criteria * Patients who refuse to co-operate * Systemic conditions of exclusion: * Medical conditions requiring prolonged use of steroids * Severe hemophilia * In therapy with intravenous bisphosphonates * History of white blood cell dysfunction or deficiency * History of head and neck radiotherapy or chemotherapy * History of kidney failure * Pregnant or breastfeeding patient * History of uncontrolled endocrine disorders * Physical handicaps that hinder proper oral hygiene * Use of experimental devices or drugs within 30 days prior to implant placement surgery * Alcoholism or drug abuse * Smokers of\> 10 cigarettes per day or the equivalent cigar or\> 10 tobacco-based chewings per day * Conditions or circumstances that prevent the completion of participation in the study or interfere with the analysis of the study results Local exclusion conditions: * Local inflammation, including untreated periodontitis * Patients with erosive lichen planus * History of local radiation therapy * Presence of bone lesions * Unhealed extraction sites * History of bone reconstruction and bone grafting techniques in the sites where the implants are to be inserted * Bruxism * Bleeding index\> 30% and number of pockets\> 5mm greater than 10

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Clinica Odontoiatrica Giorgio Vogel Milan MI Recruiting

More University of Milan trials in Italy

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 NCT05073952 on ClinicalTrials.gov ↗ ← All trials in Italy