Study of Collagen Membrane in Guided Bone Regeneration

Preliminary Study of Hypro-Sorb® F Bilayer Bioabsorbable Membrane for Guided Tissue and Bone Regeneration

Status

UNKNOWN

Phases

Phase 1Phase 2

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00454038

Acronym

GBR

Enrollment

100

Registered

2007-03-29

Start date

2007-06-30

Completion date

2009-05-31

Last updated

2009-07-10

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

Conditions

Cystectomy, Periimplantitis, Root Amputation and Apicoectomy, Segmental Growing of Alveolar Tissue, Sinus Lift

Keywords

cystectomy, augmentation, sinus, amputation, implant

Brief summary

The main purpose of this study is to investigate the efficacy of Hypro-Sorb® F, a bilayered bioabsorbable membrane in inducing bone regeneration in different dental procedures requiring GBR.

Detailed description

Guided bone regeneration is a procedure used in dentistry for the reconstruction of osseous defects around teeth, dental implants, and prior to implant placement. The main function of the membrane barrier in GBR is to mechanically prevent the undesirable penetration of epithelial cells and fibroblasts to the bone defect area, creating a secluded space where bone regeneration may occur. Resorbable and non-resorbable membranes have been used in GBR. While non resorbable membranes require another surgical procedure for removing the membrane after the healing period, the resorbable membranes have the advantage of transmitting tissue fluids, excluding undesirable cell penetration and sparing an additional unwanted surgical procedure. The aim of this study is to investigate the efficacy of Hypro-Sorb® F, a bilayered bioabsorbable membrane in inducing bone regeneration in different dental procedures requiring GBR.

Interventions

DEVICEHYPRO SORB F

resorbable, double layered, collagen membrane

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* Cystectomy * Segmental growing of alveolar tissue * Lifting of the sinus bottom * Root amputation * Apicoectomy * Filling of the alveolus after resections in prosthetic surgical practice * Periimplantitis * Maxillofacial surgery

Exclusion criteria

* Inside bone fractures when acrylate adhesives are applied.

Design outcomes

Primary

Measure	Time frame
expected	2 years

Countries

Israel

Contacts

Primary ContactEmad K Ailabouni, D.M.D

emadniss@netvision.net.il(972)46652429

Backup ContactRabab R Jarjoura, D.M.D

rababrj@yahoo.com(972)504358785

Outcome results

None listed

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