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ISQ Differences Between Different Implants in Post-extraction Sockets

U

University of Rome Tor Vergata

Status

Enrolling

Conditions

Implant Stability
Bone Healing

Treatments

Diagnostic Test: Implant stability quotient

Study type

Interventional

Funder types

Other

Identifiers

NCT06711744
TLCVSTLX

Details and patient eligibility

About

Two different implants will be used in post-extraction sockets and ISQ will be recorded monthly from insertion moment to 12 months of follow up to understand if ISQ can be affected by implant macro design

Enrollment

30 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients (at least 18 years old) presenting with failing tooth.
  • no recession of gingival contour of tooth to be extracted
  • no periodontal bone loss of neighboring teeth
  • no implants in neighboring teeth
  • class I extraction socket (intact buccal wall)
  • atraumatic extraction of the tooth with intact socket walls remaining.

Exclusion criteria

  • deep bite (severe II class)
  • systemic disease (diabetes, osteoporosis)
  • heavy smokers (more than 10 cigarettes/day)

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

30 participants in 2 patient groups

TISSUE LEVEL X
Active Comparator group
Description:
Implants with aggressive macro design
Treatment:
Diagnostic Test: Implant stability quotient
TISSUE LEVEL C
Experimental group
Description:
Implants with less aggressive macro design
Treatment:
Diagnostic Test: Implant stability quotient

Trial contacts and locations

1

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Central trial contact

Paolo Carosi, PhD

Data sourced from clinicaltrials.gov

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