comparison of effects from zirconia and titanium abutments in anterior regio
- Conditions
- Health Condition 1: K084- Partial loss of teeth
- Registration Number
- CTRI/2021/02/031227
- Lead Sponsor
- Self
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Males and females aged at least 18 years-40 years.
2.Successfully osseointegrated single tooth implant (ADIN®) inserted at least 16 weeks after tooth extraction.
3.Full mouth plaque index
1.Systemic diseases that would interfere with dental implant therapy (e.g. diabetes).
2.Any contraindications for oral surgical procedures
3.History of local irradiation therapy
4.Patients who smoke >5 cigarettes per day or tobacco equivalents or chew tobacco
5.Subjects who had undergone administration of any investigational device within 30 days of enrolment in the study
6.Conditions or circumstances in the opinion of investigator that would prevent completion of study participation or interfere with analysis of study results such as history of non-compliance
7.Physical or mental handicaps that would interfere with the ability to perform adequate oral hygiene
8.Pregnant or breastfeeding women
9.Alcohol abuse
10.Existing implants in adjacent position
11.Patients with inadequate oral hygiene or unmotivated for adequate home care
12.Probing pocket depth of >=4mm on one of the teeth immediately adjacent to the dental implant site
13.Lack of primary stability of the implant
14.Inappropriate implant position for the prosthetic requirements
15.Major simultaneous augmentation procedures
16.Insufficient stability of implant
17.Height of the abutment is <65% of the height of the complete restoration
18.Severe bruxing or clenching habits
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method