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NCT Number: NCT07001813

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

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

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Key information

Conditions

Implant Therapy

Age range

20 year–40 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

faculty of dentistry Suez canal university

Ismailia, Egypt

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

socket preserved

Device

(8 cases): was treated by immediate socket preservation with S1-XB xenograft augmentation after extraction.

non preserved socket

Device

(8 cases): was not exposed to any type of socket preservation after the extraction procedure.

Primary outcomes

  1. clinical assessment of primary stability of dental implant

    Time frame: immediately and after four months • A ratchet was used to place the implant immediately The implant stability using OSTELL device was taken immediately postoperative implant insertion and was assessed after 4 months before prothesis

    implant stability assessment by

    • rachet insertion torque
    • The implant was installed into the osteotomy site using the motorized method with the engine set at 50 rpm and 35-50 N/cm torque.
    • A ratchet was used to place the implant to the desired depth when the insertion torque was more than 35N/cm torque.
    • osstell device (ISQ) Make it possible to monitor osseointegration in a precise and objective manner.
    • Osstell helps to objectively and non-invasively determine implant stability. The prob attached to the instrument via a cable and measurements are displayed on the black lit display.
    • The device held in a right angle to the center toward the implant to be examined, the maximum deviation angle from the orthoradial direction of percussion is 45 degrees. In addition, the rod and the test surface must maintain 0.6-2.5 mm distance according to the operating instructions.
    • The implant stability using OSTELL device was taken immediately postoperative and was assessed after 4 months

  2. radiographic assessment of implant stability

    Time frame: 1.Pre-operative radiographic evaluation: before implant placement 2.Intra oral paralleling periapical direct digital radiographic procedure: immediately after placement and after four months

    • Pre-operative radiographic evaluation:

    After a healing period of four months, all the patients evaluated by Scanora 3D Cone Beam Computed Tomography scanner (CBCT) for evaluation bucco-lingual dimention, mesio-distal width, relation to neighbouring vital structures, bone density and assessment good position for implant placement.

    Post-operative Digital Radiography Assessment:

    • Intra oral paralleling periapical direct digital radiographic procedure:

    Indirect Standardized digital radiographs were achieved using KaVo Scan eXam™M One and the Rinn extension cone paralleling (XCP) periapical film holder. The KaVo Scan eXam™M One is an Intraoral digital imaging plate system (psp) system using Imaging plate which is a film-like thin, flexible, and wireless phosphorescent plate, which works as a wireless receptor.

Sponsors and collaborators

Lead sponsor

Suez Canal University

Other

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Jun 3, 2025
Registry last updated
Jun 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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