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Bone Healing in Immediate Dental Implants

Not Applicable
Completed
Conditions
Alveolar Bone Loss
Platelet Rich Plasma
Interventions
Biological: PRP injection
Device: 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
Inclusion Criteria
  • patients maintaining good oral hygiene, having adequate bone quantity at the implant site, uneventful extraction
Exclusion Criteria
  • 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
GroupInterventionDescription
PRP GroupAutomated blood cell separator to extract PRPIn this group Platelet Rich Plasma (PRP) was injected in soft tissue over surgical site.
PRP GroupPRP injectionIn this group Platelet Rich Plasma (PRP) was injected in soft tissue over surgical site.
Primary Outcome Measures
NameTimeMethod
Measurement of bone loss at baseline (12 weeks) and later at 26weeksBaseline -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
NameTimeMethod
Measurement of bone loss at baseline (12 weeks) and later at 26weeksBaseline -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

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