Evaluation of Peri-implant mucosal thickness using L-PRF under Sohns Poncho technique during second stage - A split mouth, randomized clinical trial with a six week follow up
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 24
- Locations
- 1
- Primary Endpoint
- Peri implant mucosal thickness Width of keratinized mucosa
Study Overview
Brief Summary
Patients who require implants in bilaterally edentulous mandibular back teeth region will be included in the study and implant placement will be done. After the implant is placed patient will be called after 3 months. At the time of second appointment one side a membrane which will be obtained from the patients blood will be placed during healing abutment placement and only healing abutment will be placed on the other side. Soft tissue thickness, healing and width of keratinized mucosa will be compared in two groups.
Study Design
- Study Type
- Interventional
- Allocation
- Coin toss, Lottery, toss of dice, shuffling cards etc
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 18.00 Year(s) to 70.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients who require an implant in mandibular posterior region bilaterally Patients with a minimum of 2 to 3 mm of peri implant mucosa.
Exclusion Criteria
- •Smokers Uncontrolled diabetes Severe cardiovascular problems Pregnant or lactating women.
Outcomes
Primary Outcomes
Peri implant mucosal thickness Width of keratinized mucosa
Time Frame: baseline | 7 days | 14 days | 6 weeks
Wachtel’s early healing index
Time Frame: baseline | 7 days | 14 days | 6 weeks
Secondary Outcomes
No secondary outcomes reported
