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Clinical Trials/CTRI/2021/01/030194
CTRI/2021/01/030194
Completed
N/A

Evaluation of peri implant soft and hard tissues between internal hexagonal and internal conical type of implant abutment connection- A randomised controlled trial

I0 sites44 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Health Condition 1: K084- Partial loss of teeth
Sponsor
I
Enrollment
44
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
I

Eligibility Criteria

Inclusion Criteria

  • 1\. Patient in the age group of 18years or above who will be able to understand the procedure and be able to provide informed consent to participate in it.
  • 2\. Partially edentulous in posterior region(molar and premolar).
  • 3\. Patients with simplified oral hygiene index score less than 3
  • 4\. Patients having sufficient bone to allow optimal implant placement without the need of bone augmentation or recontouring and having sufficient distaance from vital tissues(2mm).
  • 5\. Presence of keratinized tissue more than 2mm
  • 6\. Stable posterior occlusion
  • 7\. Presence of adjacent teeth (1\.5mm)

Exclusion Criteria

  • 1\. Patient with a history of systemic disease that precludes standard implant therapy.
  • 2\. Patients having parafunctional habits
  • 3\. Patient with a current daily smoking habit or chewing tobacco and with a history of drug abuse or alcoholism within past years
  • 4\. Pregnant or lactating mother

Outcomes

Primary Outcomes

Not specified

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