A clinical trial to assess the effect of change in bone levels following implant placement immediately after removal of tooth with and without socket shield (leaving a tooth root section)

Clinical and radiographic evaluation of dimensional alterations of soft and hard tissues following immediate implant placement with and without socket shield - A randomized controlled clinical trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/06/014610

Enrollment

Registered

2018-06-25

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

Health Condition 1: null- Healthy

Interventions

Intervention1: Socket shield preparation with implant placement: Following administration of local anesthesia of the treatment site, the tooth will be decoronated to the gingival level.Thereafter, wi

Eligibility

Inclusion criteria

Inclusion criteria: Systemically healthy adults who present with hopeless teeth indicated for extraction and are willing for immediate implant placement. Tooth indicated for extraction should be periodontally healthy. Non smoker

Exclusion criteria

Exclusion criteria: Systemically unhealthy Teeth with present / past periodontal disease Teeth with vertical root fractures on the buccal aspect Teeth with horizontal fractures at / below bone level Teeth with external / internal resorption of buccal part of root Patients who are pregnant, intending to conceive or breast feeding

Design outcomes

Secondary

Measure	Time 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: The soft tissue around the implant will be assessed using the Pink Esthetic Score (PES). Assessment of implant mobility and signs of peri â?? implantitis will be evaluated. Assessment of pain threshold and patient satisfaction using Visual Analogue Scale (VAS)at baseline, 3 months and at 6 months.	—

Measure

Time 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: The soft tissue around the implant will be assessed using the Pink Esthetic Score (PES). Assessment of implant mobility and signs of peri â?? implantitis will be evaluated. Assessment of pain threshold and patient satisfaction using Visual Analogue Scale (VAS)at baseline, 3 months and at 6 months.

—

Primary

Measure	Time frame
To assess the dimensional alterations in bone level (buccal plate) radiographically (CBCT) and clinically by transgingival probing at baseline, 3 months and at 6 months.Timepoint: Baseline, 3 months and at 6 months	—

Countries

India

Contacts

Public ContactDr S Muthukumar

Sri Ramachandra Medical College and Research Institute

praveen_dr@hotmail.com9884118681

Outcome results

None listed

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