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Soft and Hard Tissue Changes Following Placement of Implants Immediately after Extraction of teeth

Clinical and Radiographic Evaluation of soft and hard tissue changes following placement of Implants at socket preserved sites and immediate implant placement with and without socket shield

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019723
Enrollment
75
Registered
2019-06-18
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

Intervention1: Immeduiate Implant placement with or without socket shield: 1. Following administration of local anesthesia of the treatment site, either the tooth would be extracted and implant place

Sponsors

DrSMuthukumar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Systemically healthy adults who present with hopeless teeth indicated for extraction with type-1 extraction socket and are willing for implant placement. 2. Tooth indicated for extraction should be periodontally healthy. 3. Non smoker

Exclusion criteria

Exclusion criteria: 1. Systemically unhealthy 2. Teeth with present / past periodontal disease 3. Teeth with vertical root fractures on the buccal aspect 4. Teeth with horizontal fractures at / below bone level 5. Teeth with external / internal resorption of buccal part of root 6. Patients who are pregnant, intending to conceive or breast feeding 7. Received systematic corticosteroids, Immunosuppressive agents, radiation therapy, chemotherapy in past 2 months. 8. Subjects under Bisphosphonate therapy. 9. Subjects with allergies or sensitivity to alginate, latex. 10. Subjects participating in other clinical interventional studies.

Design outcomes

Primary

MeasureTime frame
To assess the dimensional alterations in bone level (buccal plate) radiographically (CBCT) and clinically by transgingival probing as measured using indexed stents at baseline,3, 6 and 12 months.Timepoint: To assess the dimensional alterations in bone level (buccal plate) radiographically (CBCT) and clinically by transgingival probing as measured using indexed stents at baseline,3, 6 and 12 months.—

Secondary

MeasureTime frame
To evaluate the soft tissue around the implant using the Pink Esthetic Score (PES), implant mobility and signs of peri â?? implantitis. Assessment of pain threshold and patient satisfaction using Visual Analogue Scale (VAS).Timepoint: baseline,3,6 and 12 months.—

Countries

India

Contacts

Public ContactProfSMuthukumar

Sri Ramachandra Institute of Higher Education and Research

muthukumars@sriramachandra.edu.in9884118681

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 16, 2026