MedPath

Evaluation of Free Gingival Graft Timing

Not Applicable
Recruiting
Conditions
Ridge Augmentation
Alveolar Mucosa
Registration Number
NCT06294587
Lead Sponsor
University of Alabama at Birmingham
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

Inclusion Criteria:<br><br> - • At least 18 years old<br><br> - No uncontrolled medical conditions or medications that will affect their bone<br> healing.<br><br> - Good oral hygiene is defined as a full-mouth plaque score =25%11.<br><br> - Must be able to read and understand the informed consent document.<br><br> - Has a need for implants to replace missing tooth/teeth in at least 1 quadrant<br> of the mouth.<br><br> - Insufficient alveolar ridge width for endosseous implant placement, defined as<br> 5 mm or less, as determined by bone sounding and CBCT scan.<br><br> - The patient and/or guardian is willing and able to comply with pre-operative<br> and post-operative diagnostic and clinical evaluations required.<br><br> - The patient is not pregnant or breastfeeding.<br><br>Exclusion Criteria:<br><br> - Active infectious diseases.<br><br> - Liver or kidney dysfunction/failure.<br><br> - Uncontrolled diabetes (HbA1c = 8.5).<br><br> - Active cancer treatment - such as active chemotherapy radiation therapy, or<br> radiotherapy performed within =12 months from the procedure.<br><br> - Taking medications that will affect their bone healing (for example,<br> bisphosphonates and long-term anti-inflammatory medications).<br><br> - Metabolic bone diseases that affect bone healing such as osteoporosis.<br><br> - Pregnant or lactating women (self-reported).<br><br> - Current tobacco and Marijuana smokers have 10 or more cigarettes per day, and<br> former smokers (> 10 cigarettes) who quit < 10 ago (self-reported).<br><br> - Poor oral hygiene.<br><br> - Vertical loss of bone at the edentulous ridge.<br><br> - History of periodontal disease.<br><br> - The patient is pregnant or breastfeeding

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Volumetric outcome assessment;Buccal soft tissue profile
Secondary Outcome Measures
NameTimeMethod
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