Last updated: March 16, 2022
Sponsor: Guy's and St Thomas' NHS Foundation Trust
Overall Status: Active - Recruiting
Phase
N/A
Condition
Thrombosis
Vascular Diseases
Claudication
Treatment
N/AClinical Study ID
NCT05296499
254956
Ages > 16 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria: All groups:
->16 years of age
- Consent to participate in the research study and be willing to commit to studyrequirements, including completion of questionnaires and follow up visits. Group 1:
- Venous thrombosis/obstruction involving the inferior vena cava >12 months ago.
- Symptoms of exertional dyspnoea reported by patient.
- Judged by the chief investigator as suitable for surgical intervention beforerecruitment to the study.
- Agree to adhere to therapeutic anticoagulation after surgical intervention. Group 2:
- Venous thrombosis/obstruction involving the inferior vena cava >12 months ago.
- Under the clinical care of the deep venous service for surveillance of symptoms. Group 3:
- Unilateral Iliofemoral venous thrombosis /obstruction >12 months ago.
- Judged by the chief investigator as suitable for surgical intervention beforerecruitment to the study.
- Agree to adhere to therapeutic anticoagulation after surgical intervention.
Exclusion
Exclusion Criteria: All groups:
- DVT or PE in last 12 months
- Significant or untreated left sided heart disease (eg coronary artery disease, LVdysfunction, valvular abnormalities, congenital heart disease, chronic or paroxysmalarrhythmias)
- Significant or untreated chronic lung disease (eg asthma, COPD, ILD)
- Moderate to severe renal disease
- Moderate to severe liver disease
- Peripheral arterial disease
- Significant neurological or musculoskeletal disease
- Cognitive impairment or learning disabilities
- Pregnant or planning to become pregnant in next 12 months
- Active cancer (primary, metastatic or treated within last 6 months)
- Life expectancy < 2 years or chronic non-ambulatory status.
- Any other contraindication to exercise.
- Any contraindications to MRI scanning
- Inability to provide informed consent or comply with study assessments (e.g. due tocognitive impairment, physical limitations or geographic distance). Group 4: All of the above, plus:
- Previous DVT or PE
- Known, or clinical signs of chronic venous disease as judged by the chief investigatore.g. varicose veins, leg ulcers.
Study Design
Total Participants: 56
Study Start date:
September 20, 2019
Estimated Completion Date:
April 20, 2023
Study Description
Connect with a study center
Guys and St Thomas' NHS Foundation Trust
London, SE1 7EH
United KingdomActive - Recruiting
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