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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
NA trial testing ITind device implant in BPH in 1 participant. Terminated before completion.
18 February 2021
Quick facts
| Lead sponsor | Medi-Tate Ltd. |
|---|---|
| Phase | NA |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 1 |
| Start date | 18 November 2019 |
| Primary completion | 18 February 2021 |
| Estimated completion | 18 February 2021 |
| Sites | 1 location across Germany |
Drugs / interventions tested
- ITind device implant
Conditions studied
- BPH — all drugs for BPH →
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):
-
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:
- PubMed search for NCT03994263
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for BPH
Currently open trials in the same condition.
- NCT07115147 — Blue Diode Laser Vaporization for BPH · NA · recruiting
- NCT05401032 — Proof-of-concept Study to Evaluate the Safety and Efficacy of Tryptophan in Patients with BPH. · Phase 2 · recruiting
- NCT05719220 — Effect of Group Preoperative Pelvic Floor Training for HoLEP · recruiting
- NCT05620784 — Intra-operative Loop Diuretics to Improve Same-day Discharge Rates After HoLEP · Phase 3 · recruiting
- NCT05330520 — Long Term Safety and Efficacy of Butterfly Medical Prostatic Retraction Device in Benign Prostatic Hyperplasia (BPH) Pat · NA · recruiting
Other Medi-Tate Ltd. trials
Trials by the same sponsor.
- NCT04579913 — A Multi-center, International Prospective Follow up Study · terminated
- NCT03239951 — Study to Assess the Efficacy, Safety and Tolerability of (iTind) · NA · terminated
- NCT03395522 — Study to Assess the Efficacy of the iTind in Subjects With Symptomatic BPH · NA · unknown
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03994263 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Medi-Tate Ltd.
- Last refreshed: 7 October 2021
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