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Post-Market Celect Platinum Vena Cava Filter and Gunther Tulip Retrieval Set Study

Sponsor: Cook Research Incorporated

NCT ID: NCT05881798

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Celect Platinum Vena Cava Filter (device)
How long the study runs
Study runs about 66 months (dates as stated)
About the drug or intervention
Celect Platinum Vena Cava Filter — device: Inferior vena cava filter
Patient visit burden
Not specified by the sponsor

In plain English

This study collects information about patients who have a Celect Platinum Vena Cava Filter put in place. A vena cava filter is a small device placed in a large vein to help stop blood clots, such as those linked to deep vein thrombosis (a blood clot in a deep vein) or pulmonary embolism (a blood clot in the lungs), from travelling to the lungs. The study is run by Cook Research Incorporated.

Who can take part

  • Patients who have a procedure where a Celect Platinum Vena Cava Filter is placed
  • Patients who have not taken part in the Cook MDR-2126 study before

Who may not be able to

  • Patients (or their legally authorised representative) who object to their data being collected and processed, or who are not willing to sign the informed consent form

What taking part involves

  • • Not stated — ask your trial team
  • • Not stated — ask your trial team

Time commitment: Not stated — ask the trial team, as the registry entry does not say how long the study lasts, how many visits are needed, or what taking part involves.

Plain-English summary (AI-generated) from registry data. Not eligibility advice — only the trial team can confirm whether you can take part. Use the eligibility checker to see how your health profile matches this trial.

Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
82
Started
2025-06-02
Last checked
2026-04

Plain English Summary

What is this study?

  • • Testing a new treatment for deep vein thrombosis
  • • Clinical study - 82 participants
  • • This prospective, observational, post-market study will be performed to collect patient-level data on the Celect Platinum Vena Cava Filter Sets and the Günther Tulip Vena Cava Filter Retrieval Set to confirm continued safety and performance of the devices throughout their expected lifetime and continued acceptability of the benefit:risk ratio

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with deep vein thrombosis

Where?

  • • Leeds - Leeds Teaching Hospital NHS Trust
  • • Hull - Hull University Teaching Hospitals NHS Trust
  • • Liverpool - Royal Liverpool Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

This prospective, observational, post-market study will be performed to collect patient-level data on the Celect Platinum Vena Cava Filter Sets and the Günther Tulip Vena Cava Filter Retrieval Set to confirm continued safety and performance of the devices throughout their expected lifetime and continued acceptability of the benefit:risk ratio. Additionally, the study intends to evaluate longer-term (i.e., up to 5 years) outcome data while the filter is indwelling.

Deep Vein ThrombosisVenous ThromboembolismPulmonary Embolism

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓A patient dataset is deemed suitable for inclusion if the patient has a procedure where a Celect Platinum Vena Cava...
  • ✓Subject has not previously participated in the Cook MDR-2126 study.
See the full criteria
Inclusion Criteria: * A patient dataset is deemed suitable for inclusion if the patient has a procedure where a Celect Platinum Vena Cava Filter is placed * Subject has not previously participated in the Cook MDR-2126 study. Exclusion Criteria: * Patients will be excluded from enrollment if the patient or his/her legally authorized representative objects to collection and processing of his/her data or is not willing to sign the Informed Consent.

Where Is This Study? (3 UK sites)

Leeds Teaching Hospital NHS Trust

Leeds LS1 3EX, United Kingdom

Recruiting
Hospital R&D contact (matched)

R&I Team

leedsth-tr.researchfacilitation@nhs.net0113 2060469

Hull University Teaching Hospitals NHS Trust

Hull HU3 2JZ, United Kingdom

Recruiting
Hospital R&D contact (matched)

James Illingworth

hyp-tr.development.research@nhs.net01482 461883 or 461903

Royal Liverpool Hospital

Liverpool L7 8XP, United Kingdom

Recruiting

How to Get in Touch

Sabina Andersen

Sponsor contact

CONTACT

+45 29 73 41 34 sabina.hjorth@cookmedical.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-04