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Clinical and Radiographic Assessment of the Outcomes of Dental Implant Inserted After Xenograft Socket Preservation in Posterior Maxilla

S

Suez Canal University

Status

Completed

Conditions

Implant Therapy

Treatments

Device: socket preserved
Device: non preserved socket

Study type

Interventional

Funder types

Other

Identifiers

NCT07001813
545/2022

Details and patient eligibility

About

Clinical and Radiographic Assessment of the Outcomes of Dental Implant Inserted after Xenograft Socket Preservation in Posterior Maxilla: A Randomized Controlled Study

Full description

Dental implants have become a common choice among the treatment options for missing teeth rehabilitation and has remarkably high survival and success rates Since the introduction of implants into clinical practice more than several decades ago. The success rate of dental implants, over the last ten years, has been about 90- 95%.

Invasive and non-invasive clinical tests are available like histomorphometric analysis, radiographic analysis, push- and pull-out tests, percussion tests, Periotest and resonance frequency analysis (RFA) are employed to assess the steadiness of dental implants to assess objectively implant stability at different stages of its service life to verify successful implantation.

Enrollment

16 patients

Sex

Male

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male patients aged between 21 and 40 years.
  • General good health.
  • Absence of any relevant systemic disease.
  • Presence of a hopeless maxillary posterior tooth that requires extraction.
  • Extraction site suitable for replacement by a dental implant.
  • Cases have adequate bone width and length.
  • Volunteer subjects must sign an informed consent.

Exclusion criteria

  • Poor oral hygiene with no possibility of improvement.
  • Smokers (more than 10 cigarettes per day).
  • Chronic treatment with any medication known to affect oral status and bone turnover.
  • Drug or alcohol abuse.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

16 participants in 2 patient groups, including a placebo group

socket preserved
Active Comparator group
Description:
(8 cases): was treated by immediate socket preservation with S1-XB xenograft augmentation after extraction.
Treatment:
Device: socket preserved
non preserved sockets
Placebo Comparator group
Description:
(8 cases): was not exposed to any type of socket preservation after the extraction procedure.
Treatment:
Device: non preserved socket

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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