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Immediate Implant Placement With Immediate Professionalization in Aesthetic Area

Immediate Implant Placement With Immediate Professionalization in the Maxillary Esthetic Zone Using Mixture of Allograft and Xenograft vs Xenografts to Augment the Jumping Gap

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03665025
Enrollment
2
Registered
2018-09-11
Start date
2019-01-01
Completion date
2019-01-01
Last updated
2018-09-12

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

Conditions

Implant Site Reaction

Brief summary

Immediate implant placement with immediate professionalization in the maxillary esthetic zone using mixture of allograft and xenograft vs xenografts to augment the jumping gap

Detailed description

Implant placement in fresh extraction sockets in conjunction with appropriate guided bone regeneration has many benefits, which ultimately affect the total treatment plan. The immediate placement of implants provides significant advantages, including fewer surgical procedures, shorter treatment time, and improved esthetics. The goals of osseous replacement are maintenance of contour, elimination of dead space, and reduce postoperative infection, provide good support for dental implant and enhance bony and soft tissue healing. allograft bone has gold standard over other augment techniques including favorable bone quality and minimal bone resorption.

Interventions

OTHERimmediate implant using mixed allograft and xenograft

immediate implant using mixed allograft and xenograft in anterior area to fill jumping area

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

jumping gap area in aesthetic area

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult patients with badly broken teeth in upper esthetic zone indicated for extraction, presence of at least 4 mm of bone beyond the root apex to guarantee implant primary stability, implant placement within the alveoli confines. * 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.

Design outcomes

Primary

MeasureTime frameDescription
Crestal bone loss1 yearWill be measured using calliper with scale(1-10mm) for evaluation of crestal bone loss around implant which are the lower values represent a better outcome.

Secondary

MeasureTime frameDescription
Patient satisfaction1 yearWill be measured using a satisfaction table chart which divided in 4 paraments with scale from 1-4 include( pain-infection-radiography-successful implant ),the number represent (4 excellent-3 very good -2 good-1 bad)

Countries

Kuwait

Contacts

Primary Contactmohamed hammad, BDS
dr_nucler@hotmail.com0096551553531

Outcome results

None listed

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