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EXERT: Exercise Physiology After Thrombosis

Exercise Physiology After Thrombosis (EXERT): a Prospective Single Centre Cohort Study of Cardiovascular and Exercise Physiology in Patients With Previous Venous Thrombosis in the Inferior Vena Cava and Iliofemoral Veins.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05296499
Enrollment
56
Registered
2022-03-25
Start date
2019-09-20
Completion date
2023-04-20
Last updated
2022-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Venous Thrombosis Deep (Limbs), Post Thrombotic Syndrome

Brief summary

Deep vein thrombosis (DVT) can cause long-term scarring and narrowing of veins. When there is extensive damage to the veins in the legs, groin or abdomen it can affect the way that blood is able to flow back up to the heart. Some patients are left with severe symptoms such as pain, leg swelling and ulcers, and have surgical treatment with nitinol stents to re-open the veins and relieve symptoms. The primary aim of this study is to investigate venous blood flow to the heart during exercise in patients with extensive damage to the veins in the groin and abdomen after DVT, and changes that happen after stenting.

Detailed description

Participants will have cardiopulmonary exercise testing, 6 minute walk test and basic blood tests to establish exercise tolerance and rule out other heart and lung conditions. Exercise cardiac MRI will be used to evaluate cardiac function during exercise. All participants will complete generic and disease specific quality of life questionnaires. Participants who are having a stenting procedure will repeat assessments 6-8 weeks after surgery.

Interventions

Cardiopulmonary exercise testing using cycle ergonomenter

DIAGNOSTIC_TESTExercise cardiac MRI

Exercise cardiac MRI using supine cycle, participants exercised to peak workload as determined by CPET

DIAGNOSTIC_TESTBlood tests

FBC, U&E, LFTS

OTHERQuality of life questionnaires

SF36, EQ5D, VEINES-QoL/Sym

OTHERRepeat baseline assessments

repeat baseline

DIAGNOSTIC_TESTMR venogram

MRI scan of venous system

Sponsors

King's College London
CollaboratorOTHER
Guy's and St Thomas' NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

All groups: -\>16 years of age \- Consent to participate in the research study and be willing to commit to study requirements, 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 before recruitment 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 before recruitment to the study. * Agree to adhere to therapeutic anticoagulation after surgical intervention.

Exclusion criteria

All groups: * DVT or PE in last 12 months * Significant or untreated left sided heart disease (eg coronary artery disease, LV dysfunction, valvular abnormalities, congenital heart disease, chronic or paroxysmal arrhythmias) * 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 to cognitive 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 investigator e.g. varicose veins, leg ulcers.

Design outcomes

Primary

MeasureTime frameDescription
VO2 max after stenting6-8 weeks post surgeryAs determined by cardiopulmonary exercise testing
Peak cardiac output during exercise6-8 weeks post surgeryas determined by exercise cardiac MRI

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026