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Evaluation of Dental Implants Placed in Preserved and Non-preserved Post-extraction Ridges

R

Rio de Janeiro State University

Status

Withdrawn

Conditions

Platelet-rich Fibrin
Alveolar Rege Preservation
Dental Implant Failed
Alveolar Bone Loss

Treatments

Device: Dental implant

Study type

Observational

Funder types

Other

Identifiers

NCT03715439
72596717.3.0000.5259/2

Details and patient eligibility

About

A prospective study to evaluate and compare implants placed in preserved versus non-preserved extraction sockets using L-PRF (Leucocyte- and platelet-rich fibrin) after 1, 3 and 5 years.

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Health patients, American Society of Anesthesiologists (ASA) I or II
  • Patients who need to submit tooth extraction (pre-molar, canine and incisor teeth which present ideal conditions to receive dental implants after 3 months.

Exclusion criteria

  • Systemic diseases related with healing disorders
  • Poor oral hygiene
  • Pregnant or lactating patient
  • Use of flap elevation for dental extraction

Trial design

0 participants in 2 patient groups

Leucocyte- and Platelet-rich Fibrin
Description:
Dental implant placed into post-extraction sites preserved with leucocyte- and platelet-rich fibrin
Treatment:
Device: Dental implant
Control
Description:
Dental implant placed into non-preserved post-extraction sites
Treatment:
Device: Dental implant

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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