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Clinical Trials/CTRI/2025/04/085712
CTRI/2025/04/085712CompletedNot Applicable

Evaluation of marginal bone loss and esthetic outcome for socket shield technique and immediate implant placement in maxillary premolar region. An in-vivo study.

pankaj kadam1 site in 1 country24 target enrollmentStarted: May 10, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
24
Locations
1
Primary Endpoint
There is no change in marginal bone loss and aesthetic outcome in socket shield technique and immediate implant placement in maxillary premolar region

Study Overview

Brief Summary

The purpose of the study is to rehabilitate the petients tooth with dental implants and maintain periimplant bone and soft tissue.  Participants will be selected based on the patients dental health and will be treated with one of the two techniques that is either socket shield technique or immediate implant placement technique depending upon the retained dental root which is previously indicated for extraction.

Study Design

Study Type
Interventional
Allocation
Na
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 50.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1 Teeth indicated for extraction and which cannot be restored.
  • 2 Teeth with healthy periodontal status with no gingival inflammation or bone loss.
  • 3 Adequate palatal/lingual and apical bone for implant placement.
  • 4 Favorable occlusal scheme for immediate provisional and definitive restoration.
  • 5 For multirooted teeth, having large interradicular bone.
  • 6 All patients included in the study should have one missing posterior tooth, with adjacent or contralateral sound natural teeth without any carious lesions, trauma or wasting disease.
  • 7 Patients who are willing to involve in the study.

Exclusion Criteria

  • 1 Mobile teeth.
  • 2 Teeth with thin or absence of labial and palatal bone.
  • 3 Teeth with larger periapical infection or any active lesion.
  • 4 Vertical root fracture.
  • 5 Internal resorption.
  • 6 Patients having habit of smoking and chewing tobacco.
  • 7 Patients having systemic diseases like uncontrolled diabetes, hypertension and bleeding disorders.
  • 8 Patients who are not physically fit for the treatment as consulted by the physician.
  • 9 Pregnant woman and lactating mothers.
  • 10 Patients who have undergone radiation therapy.
  • 11 Patients with parafunctional habits, restored adjacent or contralateral tooth, or acute infection at the implant region.

Outcomes

Primary Outcomes

There is no change in marginal bone loss and aesthetic outcome in socket shield technique and immediate implant placement in maxillary premolar region

Time Frame: baseline 3 months 6 months 9 months

Secondary Outcomes

  • There is no change in maginal bone loss & aesthetic outcome in socket shield technique & immediate implant placement in maxillary premolar region at the end of 9 months.(at the end of 9 months)

Investigators

Sponsor
pankaj kadam
Sponsor Class
Other [self funded]
Responsible Party
Principal Investigator
Principal Investigator

pankaj kadam

KLE VK institute of dental sciences, belgaum

Study Sites (1)

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