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NCT04054219

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

Status unknown NA Last updated 21 August 2019
What this trial tests

NA trial testing Bone graft substitute in Bone Loss in Jaw in 47 participants. Status unknown.

Timeline
8 July 2019
Primary endpoint
28 February 2020
31 May 2021

Quick facts

Lead sponsorWishbone SA
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment47
Start date8 July 2019
Primary completion28 February 2020
Estimated completion31 May 2021
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Wishbone SA

Who can join

Adults 18 to 80, any sex, with Bone Loss in Jaw. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Bone graft substitute

Trials testing the same drug.

Other recruiting trials for Bone Loss in Jaw

Currently open trials in the same condition.

Other Wishbone SA trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04054219.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing