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Peri-implant tissue response to PEEK and Titanium implant abutments: An In-vivo Six Months Randomized Controlled Clinical Study.

Comparative evaluation of soft and hard tissue parameters and inflammatory biomarker around customized titanium and polyether-ether-ketone dental implant abutment â?? A clinical,radiological and biochemical study. - RCT

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019545
Enrollment
30
Registered
2019-06-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Control Intervention1: PEEK dental implant abutment: Comparisons of plaque index (mPII), sulcular bleeding index (SBI), probing depth (PD) and crestal bone level (CBL) and Interleukin IL-1beta cytokin

Sponsors

Manika Mittel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects having good systemic health and mental condition maintaining optimum oral hygiene care, with the presence of adequate bone volume and inter-arch space to accommodate implant prosthesis of appropriate size, with stable occlusal relationship and available for 1 year of investigations were included in the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria were: Subjects having systemic diseases (diabetes mellitus, rheumatoid arthritis, cardiovascular diseases, etc.) that would preclude surgical procedure, physical and mental disabilities that would conflict with the capability to perform adequate oral hygiene, pregnant and lactating mothers; insufficient bone volume requiring augmentation of the implant site; active infection or severe inflammation in the areas intended for implant placement; subjects currently receiving intravenous or oral bisphosphonate therapy; subjects with severe bruxism or clenching habits; treatment with therapeutic radiation to the head region within the past 12 months; alcohol or drug abuse and smoking

Design outcomes

Primary

MeasureTime frame
Clinical evaluation of peri-implant soft and hard tissue parameters, radiological and biochemical examinations of the reconstructions will be performed immediately after crown insertion baseline, at 12 weeks and at 24 weeks of function.Timepoint: Clinical evaluation of peri-implant soft and hard tissue parameters, radiological and biochemical examinations of the reconstructions will be performed immediately after crown insertion baseline, at 12 weeks and at 24 weeks of function.

Secondary

MeasureTime frame
Clinical evaluation of peri-implant soft and hard tissue parameters, radiological and biochemical examinations of the reconstructions will be performed immediately after crown insertion baseline, at 12 weeks and at 24 weeks of function.Timepoint: Clinical evaluation of peri-implant soft and hard tissue parameters, radiological and biochemical examinations of the reconstructions will be performed immediately after crown insertion baseline, at 12 weeks and at 24 weeks of function.

Countries

India

Contacts

Public ContactManika Mittel

Inderprastha Dental College and Hospital

drmanika29@gmail.com9818161022

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026