CTRI/2024/05/067565
Not yet recruiting
Phase 4
A Comparative Evaluation of Mean Crestal Bone Level Changes among Hydrophobic, Hydrophilic, and Laser Micro-Grooved Dental Implants Post 1 Year of Immediate Loading – A Randomised Clinical Control Trial. - NI
self funding0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: K068- Other specified disorders of gingiva and edentulous alveolar ridge
- Sponsor
- self funding
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male or female patients with age group between 25 to 60 years
- •Patients not contraindicated for periodontal or implant surgery
- •One bounded edentulous space ie a single tooth missing with intact proximal teeth primarily in the lower posteriors premolars and molars with sufficient bone quantity to allow implant placement
- •Patients should be cooperative motivated and oral hygiene conscious
- •Sufficient bone height at least 13mm and sufficient bone width at least 6mm should be present
- •Presence of local factors without signs of clinical inflammation
- •Stable occlusion with no para functional habits
Exclusion Criteria
- •Presence of active periodontal disease at the time of implant surgery
- •Patients who did not accept to comply for 1 year follow\-up were excluded from the study
- •Patient diagnosed with known systemic diseases Bone disorders like hyperparathyroidism osteoporosis or Pagets disease
- •Patients who are under steroids antiinflammatory and bisphosphonates in the past 6 months
- •Patients who are treated with radiotherapy or chemotherapeutic agents.
- •Chronic alcoholics or drug abuse
Outcomes
Primary Outcomes
Not specified
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