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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03584997
Other study ID # 5050
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date July 1, 2019

Study information

Verified date July 2018
Source Cairo University
Contact Mohammed D Darwish, Masters
Phone 00201206036565
Email doctorelsayed87@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Histological Measurement Comparing the density of the new bone formed during socket preservation technique using a Mixture of Anorganic Bovine Bone(ABB) And Autogenous Particulate vs a Mixture of Injectable Platelets Rich Fibers, ABB And Autogenous Particulates (sticky bone). radiographical measurements of the amount of bone dimensions changes in socket preservation technique in 6-month period using a Mixture Of Anorganic Bovine Bone(ABB) And Autogenous Particulate vs a Mixture Of Injectable Platelets Rich Fibers, ABB And Autogenous Particulates (sticky bone)


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date July 1, 2019
Est. primary completion date December 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- Adult patients with hopeless mandibular molars indicated for extraction and implant placement in two stages that indicate socket preservation.

- Both sexes.

- No intraoral soft and hard tissue pathology.

- No systemic condition that contraindicate implant placement.

Exclusion Criteria:

- Presence of fenestrations or dehiscence of the residual bony Walls after extraction.

- Heavy smokers more than 20 cigarettes per day .(24)

- Patients with systemic disease that may affect normal healing.

- Psychiatric problems

- Disorders to implant are related to history of radiation therapy to the head and neck neoplasia, or bone augmentation to implant site.

- Patients that refuse to be called back for implant placement post extraction.

- Patients that have exceeded bone resorption surrounding the tooth prior to extraction and require guided bone regeneration.

Study Design


Intervention

Procedure:
ABB And Autogenous Particulate
Mixing the autogenous bone graft aquired at the time of surgery with a 50:50 ration of anorganic bovine bone and filling the socket
PRF, ABB & Autogenous Particulate
adding an injectable platelets rich fibrin to a Mixture of autogenous bone graft aquired at the time of surgery with a 50:50 ration of anorganic bovine bone and filling the socket

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary histomorphometrical bone quality histological bone quality measured from a core sample taken from the grafted site 6 month
Secondary marginal bone loss alveolar margin bone loss measured be CBCT 6 month
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