Clinical Trials Directory

Trials / Unknown

UnknownNCT04054219

Evaluation of Efficacy and Safety of Wishbone HA as Bone Graft Substitute, a Pre-market Clinical Investigation

Prospective, Single Center, Pivotal Investigation to Investigate Efficacy and Safety of WISHBONE HA, Used as Bone Graft Substitute for Different Indications Where Bone Grafting Procedures Are Required Before Implant Placement.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
47 (estimated)
Sponsor
Wishbone SA · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

Evaluation of efficacy and safety of Wishbone HA as bone graft substitute, a pre-market clinical investigation. Group1: Extraction Socket management Group 2: Sinus lift

Conditions

Interventions

TypeNameDescription
DEVICEBone graft substituteEvaluation of a device made of deproteinized bovine bone material as bone graft substitute in different indications requiring bone grafting procedures before implant placement

Timeline

Start date
2019-07-08
Primary completion
2020-02-28
Completion
2021-05-31
First posted
2019-08-13
Last updated
2019-08-21

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT04054219. Inclusion in this directory is not an endorsement.

Evaluation of Efficacy and Safety of Wishbone HA as Bone Graft Substitute, a Pre-market Clinical Investigation (NCT04054219) · Clinical Trials Directory