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A Study To Evaluate Clinical And Radiographic Effect Of UV Irradiated Sandblasted Large Grit And Acid Etched Surface Implant on Implant Stability And Marginal Bone Loss In Edentulous Maxillary Posterior Region

Clinical Effect Of UV Irradiated Sandblasted Large Grit And Acid Etched Surface Implant On Implant Stability And Marginal Bone Loss In The Maxillary Posterior Region A Parallel Randomised Double Blind Clinical Trial - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105493
Enrollment
70
Registered
2026-03-06
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: - Health Condition 2: 8- Other Procedures

Interventions

Intervention1: uv treated group: After evaluation of pretreatment records and anatomical landmarks, patients will be prepared for implant placement under aseptic conditions using povidone iodine an

Sponsors

Darshan Khairnar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Good oral hygiene and suitability for implant placement. 2.Sufficient bone height and width to receive the implant. 3.Edentulous area in the maxillary posterior region. 4.Healed extraction sockets with a history of extraction minimum 6 months ago. 5.Systemically healthy patient. 6.Patients willing to and fully capable of complying with the study protocol

Exclusion criteria

Exclusion criteria: 1.Patients who are not cooperating and with systemic co-morbidities that are likely to affect the study outcome (uncontrolled diabetes mellitus, immunocompromised patients, psychological problems, radiotherapy of head and neck region within the past 24 months). 2.Severe periodontal problems. 3.Conditions requiring bone graft. 4.Chronic alcoholism, and smoking. 5.When bone or soft tissue regeneration was needed to enhance implant stability or esthetics. 6.Patients under medication which are likely to affect the treatment outcome. 7.Presence of any parafunctional habits. 8.Pregnant or lactating females.

Design outcomes

Primary

MeasureTime frame
To evaluate the clinical effect of photofunctionalization on implant stability in the maxillary posterior region.Timepoint: baseline,4 weeks and 4 months

Secondary

MeasureTime frame
To evaluate the radiographic effect of UV irradiated SLA surface implant on marginal bone loss in the maxillary posterior regionTimepoint: baseline,4 months and 1 year

Countries

India

Contacts

Public ContactDarshan Khairnar

S. C. B. Dental College And Hospital Cuttack Orissa, India

drsubash007@gmail.com9437008298

Outcome results

None listed

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