NCT03414515 is a clinical trial of Endovascular intervention in Peripheral Arterial Disease, sponsored by Duomed.

Who is sponsoring NCT03414515?

NCT03414515 is sponsored by Duomed.

What drugs are being tested in NCT03414515?

Interventions in NCT03414515: Endovascular intervention.

What condition does NCT03414515 study?

NCT03414515 studies Peripheral Arterial Disease, Iliac Artery Disease, Femoropopliteal Occlusive Disease, Below-the-knee Obstruction.

Is NCT03414515 still recruiting?

NCT03414515 is currently completed. Last updated 5 September 2024.

Last reviewed 2024-09-05 · How we verify

NCT03414515

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Endovascular Treatment of Peripheral Artery Disease (PAD)

Completed Last updated 5 September 2024

What this trial tests

trial testing Endovascular intervention in Peripheral Arterial Disease in 200 participants. Completed in 1 December 2021.

Timeline

2 May 2018

Primary endpoint
1 December 2021

1 December 2021

Quick facts

Lead sponsor	Duomed
Status	Completed
Study type	OBSERVATIONAL
Enrollment	200
Start date	2 May 2018
Primary completion	1 December 2021
Estimated completion	1 December 2021
Sites	1 location across Belgium

Drugs / interventions tested

Endovascular intervention

Conditions studied

Peripheral Arterial Disease — all drugs for Peripheral Arterial Disease →
Iliac Artery Disease — all drugs for Iliac Artery Disease →
Femoropopliteal Occlusive Disease — all drugs for Femoropopliteal Occlusive Disease →
Below-the-knee Obstruction — all drugs for Below-the-knee Obstruction →

Sponsor

Duomed

Who can join

18 and older, any sex, with Peripheral Arterial Disease or Iliac Artery Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this observational study is to evaluate the performance and safety of endovascular treatment with stenting (Optimed Sinus Superflex 635 or Qualimed Pontos-pp) or balloon angioplasty (Cardionovum Legflow or Optimed Nylotrack .035 + .018) according to current practice. The goal of the study will be achieved by assessing binary restenosis with duplex ultrasound, peri- and postoperative complications, technical success, target lesion revascularization, amputation and clinical outcome.

Publications & conference data

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

Angioplasty versus stenting for iliac artery lesions.
Jongsma H, Bekken J, Ayez N, Hoogewerf CJ, et al · · 2020 · cited 12× · PMID 33258499 · DOI 10.1002/14651858.cd007561.pub3

Verify or expand the search:

Other trials of Endovascular intervention

Trials testing the same drug.

NCT04219774 — NeuroCognition After Carotid Recanalization · Phase 2 · completed

Other recruiting trials for Peripheral Arterial Disease

Currently open trials in the same condition.

NCT05437562 — Randomized Clinical Trial for Ewing Amputation in the VA · NA · recruiting
NCT07427108 — Road Mapping Guided Puncture Versus Ultrasound Guided Puncture During Retrograde Angioplasty Feasibility and Safety · NA · recruiting
NCT07336381 — Replexa+ Shortwave Diathermy Device for Patients Diagnosed With Peripheral Artery Disease and Peripheral Neuropathy · NA · recruiting
NCT07076082 — Vascular Trial Associated Registry Pilot · Phase 4 · recruiting
NCT06308562 — Fuzzy Wale Compression Stockinet to Promote Healing Following Transtibial Amputation for Peripheral Arterial Disease · NA · recruiting

Other Duomed trials

Trials by the same sponsor.

NCT04808206 — A Registry of Laparoscopic Bariatric Surgery Using Stapling Devices: Observation of Safety and Clinical Efficacy · active not recruiting
NCT04543526 — A Post-market Observational Study With the easyEndoTM Universal Linear Cutting Stapler in Standard Laparoscopic and Robo · withdrawn
NCT04564677 — A Study Evaluating the Clinical Outcome of a Modified d'Hoore Technique for Laparoscopic Ventral Mesh Rectopexy · unknown
NCT04422236 — A Post-market, Observational Registry With the easyEndoTM Universal Linear Cutting Stapler in Laparoscopic Bariatric Sur · active not recruiting
NCT03968757 — Assessing the Safety and Performance of the easyEndoTM Universal Linear Cutting Stapler in Laparoscopic Gastric Bypass S · completed

Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT03414515 (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 Duomed
Last refreshed: 5 September 2024

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/NCT03414515.

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