Autopsy report · NCT02766842

Evaluation of a New EUS Guided Biopsy Needle (SharkCore) Comparing to Standard EUS Needle (ProCore)

“The reason was the fact that the ProCore needle was removed from clinical use”

The sponsor’s own words in the registry.

Life of this trial

• Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.

Vital statistics

Status

Withdrawn

Phase

Phase 2

Sponsor

Johns Hopkins University

Sponsor type

University, hospital or other

Conditions

Mesenchymal Tumor; Autoimmune Pancreatitis; Lymphoma; Solid Tumors

Interventions

EUS-FNB with ProCore needle; EUS-FNB with SharkCore needle; ProCore needle; SharkCore needle

Participants

0

Sites

1

Countries

United States

Look deeper

• The official registry record (the source of truth)
• Record history: every change the sponsor made
• Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.