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NCT03994263

A Prospective Study to Observe the Mechanism of Action of the MediTate iTind in Subjects With Symptomatic BPH With MRI

Terminated NA Last updated 7 October 2021
What this trial tests

NA trial testing ITind device implant in BPH in 1 participant. Terminated before completion.

Timeline
18 November 2019
Primary endpoint
18 February 2021
18 February 2021

Quick facts

Lead sponsorMedi-Tate Ltd.
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment1
Start date18 November 2019
Primary completion18 February 2021
Estimated completion18 February 2021
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Medi-Tate Ltd.

Who can join

40 and older, male only, with BPH. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A total of up to 15 eligible subjects will be enrolled into this open-labeled one-arm study designed to observe the mechanism of action of iTind when using MRI

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. iTIND: the second-generation temporary implantable nitinol device for minimally invasive treatment of benign prostatic hyperplasia.
    Balakrishnan D, Jones P, Somani BK. · · 2020 · cited 11× · PMID 32655690 · DOI 10.1177/1756287220934355

Verify or expand the search:

Other recruiting trials for BPH

Currently open trials in the same condition.

Other Medi-Tate Ltd. 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/NCT03994263.

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