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Socket Preservation for Dental Implant Site Development.

Socket Preservation for Dental Implant Site Development.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03112772
Enrollment
100
Registered
2017-04-13
Start date
2017-03-20
Completion date
2017-11-20
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Loss

Brief summary

Changes in alveolar bone following teeth extraction can compromise implant placement. Socket preservation (alveolar ridge preservation) is considered as a surgical procedure employed to preserve the ridge volume within the envelope existing at the time of extraction.The ultimate aim of such procedure is to compensate the expected amount of horizontal and vertical alveolar bone resorption. In order to better understand which socket preservation materials might be more effective for ridge preservation and to strengthen the evidence that is relevant to the clinicians' choice of socket preservation materials, two different materials were compared in a randomized controlled approach. (1) Demineralized Bone Matrix (DBM) Putty and Putty with Chips allograft covered by collagen membrane, and (2) Deprotonated bovine bone xenograft covered by collagen membrane. The independent variable is the grafting material while the dependent variables are the change in socket height, and width; the ability of implant placement without the need for grafting and the success rate of implants at the time of loading.

Interventions

OTHERPuros® Allograft

It is a type of bone grafting materials used for enhancing bone formation

OTHERCopiOs® Cancellous Particulate

It is a type of bone grafting materials used for enhancing bone formation

Sponsors

Imam Abdulrahman Al Faisal Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Adult patient \> 18 years old. 2. Single and or multi-rooted teeth that are non-restorable. 3. Patients are keen to have implant placement at the extraction sites after 4 months of extraction. 4. Intact buccal bone after extraction, which was confirmed by visual inspection and clinical examination using a periodontal probe. 5. Patients are medically fit with no underlying systemic diseases.

Exclusion criteria

1. Pregnant females. 2. Smokers. 3. Presence of any acute infection at the time of teeth extraction.

Design outcomes

Primary

MeasureTime frameDescription
Width of alveolar ridge4 monthsThe distance from the buccal to the lingual surface of the alveolar ridge
height of the alveolar ridge4 monthsThe distance from the crest of the ridge to the base of the socket
Need of further grafting at the time of implant placement4 monthsAbility to place implants

Secondary

MeasureTime frameDescription
Osseintegration of implants4 monthsImplant loss before restoration

Countries

Saudi Arabia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026