Can a Lab-Grown vein with a Built-In valve fix damaged leg veins?

NCT ID NCT03784131

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 27, 2026 · Last updated Aug 28, 2026 · Updated 1 time

Summary

This trial tests whether a personalized tissue-engineered vein, made in the lab with a functioning valve, can safely replace a damaged vein segment in people with severe chronic venous insufficiency. Each participant undergoes surgery to swap a non-working valve in their femoral vein for the engineered one. Researchers monitor for complications like blood clots, infections, and surgical problems, and also track changes in symptoms. The goal is to see if this approach is safe and feasible before larger studies.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A personalized tissue-engineered vein with a functioning valve, implanted surgically to replace a damaged vein segment.
What this could lead to
If it works, this could offer a new way to repair damaged leg veins and ease symptoms like pain, swelling, and ulcers in people with chronic venous insufficiency.
What could go wrong
This is a very early, first-in-human study with only 11 participants. The vein could clot, become infected, or fail to work, and the surgery itself carries risks.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

11 people

The number who actually took part.

Started

Dec 2021

Finished

Jun 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients aged between 18 and 75 years (inclusive) * CVI patients with painful swelling and/or skin changes and/or recurrent leg ulcer despite optimal conservative treatment for a period of time according to the investigator's judgement * Patients with deep venous reflux (grade 3 and above) * Meeting ASA (American Society of Anesthesiologists Classification) class 1 or 2 according to the PIs criteria * Laboratory values * INR \<1.7 (in case the patient uses Warfarin, the test might be repeated after the anticoagulant change) * Platelets ≥ 100 x 10 9 /L * Hemoglobin ≥ 100 g/L * Total bilirubin ≤ 1.5 × upper limit of normal (ULN) * ASAT ≤ 2.5 × ULN * ALAT ≤ 2.5 × ULN * Ability to understand the requirements of the study, give direct or representative written informed consent, and comply with the study procedures Exclusion Criteria: * Patients incapable to give direct or representative written informed consent * Patients unlikely to cooperate fully in the study and/or with an anticipated poor compliance * Non-walking patients or patients with lost ankle joint function * Patients previously organ-transplanted * Patients with cancer except in-situ stage cancer (basal-cell carcinomas and/or cervix cancer) and five year recurrence free period after treatment * Patients with autoimmune diseases including rheumatoid arthritis, SLE and MS * Pregnant or breast feeding women * Patients with ongoing estrogen treatment for example for contraception. Alternative contraceptive methods (e.g. intrauterine device, bilateral tubal occlusion, vasectomized partner, sexual abstinence) should be used by women of reproductive age (defined as pre-menopausal female capable of becoming pregnant). * BMI ≥ 35 * Patients who have participated in other clinical trials during the last 12 months * Patients with artery pathology (ankle-brachial pressure index \< 0,9 or \> 1,3) * Patients with thrombophilia according to the laboratory results at inclusion visit. One of the following criteria is needed for thrombophilia: Protein C \< 40% or Protein S \< 40 % or Leiden factor mutation or Antithrombin III \< 40 % or present Lupus anticoagulant or Homocysteine \> 1.5 ULN * Patients with an active infection requiring systemic antibiotic treatment * Patients with clinically significant cardiac disease (New York Heart Association, Class III or IV) or measured LVEF 40% * Patients with uncontrolled hypertension * Patients with renal dysfunction eGFR \< 45 ml/min (according to the MDRD calculation) * Patients with moderate or severe hepatic impairment (Child Pugh ≥ 7 points, i.e. class B or C) * Patients with ongoing immunosuppression, systemic Cortisol treatment etc. * Less than 3 months since previous ipsilateral venous intervention (e.g. Iliac recanalization) * Clinically significant iliocaval stenosis or occlusion * Current smoker of more than 20 cigarettes per day * Other uncontrolled intercurrent illness that would jeopardize the patient's safety, interfere with the objectives of the protocol, or limit the patient's compliance with study requirements, as determined by the Investigator in consultation with the Sponsor * Patients with severe SARSCoV-2 virus infection requiring hospitalization in the past 6 months

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Junta de Andalusia

    Seville, Spain

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