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Clinical Trials/NCT04744012
NCT04744012CompletedNot Applicable

Modified Periostal Pocket Flap Technique: a Case Series

Universidad Complutense de Madrid0 sites8 target enrollmentStarted: September 11, 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
8
Primary Endpoint
Volume of bone augmentation

Study Overview

Brief Summary

The aim of this study is to propose a modification of the original periostal pocket flap technique consisting in replacing the xenograft by a conglomerate which contains autologous bone obtained from the future implant site through biological drilling technique and PRGF (Plasma Rich in Growth Factors)

Detailed Description

Materials and methods

8 patients referred for implant placement and with a slight bucco-lingual (BL) width deficiency in alveolar bone were included in the study. Patients were placed dental implants and bone width was augmented by using the conglomerate mentioned above.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patients with a favorable bone density and favorable bone length but insufficient bone width that could compromise implant placement

Exclusion Criteria

  • Smokers (>10 cigarettes per day) and patients with severe systemic disease ( ASA III or IV - American Society of Anaesthesiology)

Outcomes

Primary Outcomes

Volume of bone augmentation

Time Frame: 4 months

Volume of bone augmentation of the surgical sites was measured in the postoperative parasagittal CT scans using a region of interest (ROI) containing the entire bone box regenerated area using the closed polygon tool of the OsiriX software

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jesús Torres García Denche

Associate Professor

Universidad Complutense de Madrid

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