Keratized Mucosa in CG Implant Placement: CTG vs Flapless
Recruiting
N/AInterventional Study
Variation of Keratinized Mucosa After Implant Surgery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
44 (estimated)
Sponsor
University of Milan · Other
Who this trial is looking for
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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.
Trial Locations
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Status
Eligibility Criteria
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 …
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
Contacts
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