Evaluation of Gingival Dimension After Two Different Techniques for Second Stage of Implant Surgery
Not Applicable
- Conditions
- Gingival recession.Gingival recession (generalized)(localized)(postinfective)(post-operative)
- Registration Number
- IRCT201409175305N4
- Lead Sponsor
- Vice Chancellor for Research, Kerman University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Presence of sufficient keratinized gingiva, as at least 9mm of keratinized tissue would be available; Absence of bone loss assessed through periapical radiography prior to the second stage of implant surgery; Patient cosent
Exclusion criteria:
Patient's incompliance
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Keratinized gingiva dimension. Timepoint: At surgery time, and then weekly for four weeks post surgery. Method of measurement: By periodontal probe.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: One week after surgery. Method of measurement: Visual analogue scale (VAS).
Related Research Topics
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What molecular mechanisms underlie keratinized gingiva preservation using diode laser versus punch technique in IRCT201409175305N4?
How does diode laser compare to punch technique in managing localized vs. generalized post-operative gingival recession?
Are there biomarkers predicting keratinized tissue response to diode laser exposure in implant surgery trials?
What adverse events are associated with diode laser use in second-stage implant surgery for gingival recession?
What combination therapies or adjunctive materials enhance keratinized gingiva outcomes in implant exposure techniques?