Bone Healing in Immediate Dental Implants
- Conditions
- Alveolar Bone LossPlatelet Rich Plasma
- Interventions
- Biological: PRP injectionDevice: Automated blood cell separator to extract PRP
- Registration Number
- NCT04650763
- Lead Sponsor
- CMH Lahore Medical And Dental College
- Brief Summary
To study the effect of platelet-rich plasma concentrate on marginal bone loss and bone mineral density in immediate implant placement through CBCT.
- Detailed Description
12 subjects were equally categorized into two groups. Group, I was the control group; whereas, the subjects in Group II received Platelet Rich Plasma (PRP) therapy. All subjects were given a standard treatment with single implant system. Inserted implants were analyzed through Cone Beam Computerized Tomography (CBCT). Records were registered at the baseline, at 12th week before functional loading and 26th week after functional loading.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 12
- patients maintaining good oral hygiene, having adequate bone quantity at the implant site, uneventful extraction
- Active infection around implant site, immunocompromised state, with current major systemic disease (uncontrolled diabetes, rheumatoid arthritis, etc.) or oral pathologies, history of bleeding disorders or on anticoagulant therapy, or patients on bisphosphonates were excluded from the study
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description PRP Group Automated blood cell separator to extract PRP In this group Platelet Rich Plasma (PRP) was injected in soft tissue over surgical site. PRP Group PRP injection In this group Platelet Rich Plasma (PRP) was injected in soft tissue over surgical site.
- Primary Outcome Measures
Name Time Method Measurement of bone loss at baseline (12 weeks) and later at 26weeks Baseline -before functional loading at 12 weeks & at 26 weeks- after functional loading to assess changes in marginal bone loss in sagittal view using CBCT Measurement at mesial in mm
- Secondary Outcome Measures
Name Time Method Measurement of bone loss at baseline (12 weeks) and later at 26weeks Baseline -before functional loading at 12 weeks & at 26 weeks- after functional loading to assess changes in marginal bone loss in sagittal view using CBCT Measurement at distal in mm
Trial Locations
- Locations (1)
Institute of Dentistry; CMH Lahore Medical College
🇵🇰Lahore, Punjab, Pakistan