None listed
Conditions
Interventions
Intervention1: Nil: Nil
Sponsors
Sri Hasanamba Dental college and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: Patients within age group of 20 to 50 years There should be absence of any systemic diseases Implant diameter ranging from 3.5 to 4.5mm Implant length ranging from 10 to 13mm Bone quality with D1 to D3 density Implant placed in the mandibular molars with customized anatomical abutment crowns and standard abutment crowns
Exclusion criteria
Exclusion criteria: Age less than 20 years and not more than 50 years Individuals presenting with uncontrolled systemic diseases or under medications interfering with bone metabolism affecting osseointegration Subjects using narcotics alcohol or tobacco in any form Handicaps that would interfere with the ability to perform adequate oral hygiene Individuals who are immune compromised or on long term steroid therapy Patients having para functional habits Local factors like history of local inflammation untreated periodontitis mucosal diseases local irradiation therapy unhealed extraction sites Patients who refuse to undergo necessary follow up Patients with mucosal lesions affecting alveolar mucosa and gingiva Patients with failed implants or peri implantitis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of the study will be the evaluation and comparison of marginal bone level changes around implants restored with standard abutment crowns and customised abutment crowns in mandibular molar implant cases. Marginal bone level will be assessed radiographically using standardized intraoral periapical radiographs, measuring the distance from the implant platform to the first bone-implant contact on the mesial and distal aspects of the implant. The measurements will be recorded at baseline and at predetermined follow-up intervals to determine the amount of marginal bone loss and to compare the outcomes between the two groups.Timepoint: Baseline 3 6 and 12th month | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes of the study will include the assessment of peri-implant soft tissue esthetics using the Pink Esthetic Score (PES) and the evaluation of patient satisfaction. The Pink Esthetic Score will be used to analyze peri-implant soft tissue parameters such as mesial papilla, distal papilla, soft tissue level, contour, color, and texture around the implant restoration. Patient satisfaction will be assessed using a structured questionnaire or visual analog scale to evaluate factors such as comfort during mastication, esthetic appearance, ease of cleaning, and overall satisfaction with the implant-supported crown. These outcomes will help determine the esthetic and patient-reported differences between standard abutment crowns and customised abutment crownsTimepoint: Baseline 3 6 and 12th month | — |
Countries
India
Contacts
Public ContactKiran Kumar H S
Sri Hasanamba dental college and hospital
Outcome results
None listed