Compression Hosiery to Avoid Post-Thrombotic Syndrome

Not Applicable

Terminated

• Conditions: Deep Vein Thrombosis Leg; Post Thrombotic Syndrome; Deep Vein Thrombosis
• Interventions: Device: Graduated compression stocking

• Registration Number: NCT04103112
• Lead Sponsor: Imperial College London

Brief Summary

Patients with a deep vein thrombosis (DVT) may develop long-term symptoms, e.g. lifelong leg pain, skin changes and occasionally ulceration, known as post-thrombotic syndrome (PTS). This affects about half of people with a history of DVT.

This randomised study aims to show whether the regular use of a compression stocking after DVT in the leg, prevents long-term pain, swelling and ulceration. Currently small trials show varied results and a large trial is required to answer the question.

Detailed Description

Every year 1 in 1000 persons in the United Kingdom are diagnosed with a blood clot in the leg veins (deep vein thrombosis). In just under half of those with deep vein thrombosis, leg pain, swelling and skin breakdown (ulcers) can occur, a lifelong condition called post-thrombotic syndrome. This impacts upon a person's ability to work, their confidence and independence. In most patients there is no effective treatment and they lose income from unemployment. Ulcers, if they occur, require bandaging that needs to be changed twice weekly.

Treatment guidelines for deep vein thrombosis do not currently include the use of a compression stockings. They can sometimes be difficult to put on for those who cannot bend down, the stockings can slip or roll down, or become uncomfortable in hot weather. Stockings cost the National Health Service (NHS) approximately £50 every 6 months. The evidence for stockings comes from two early trials comparing patients wearing a stocking to those who did not.

There was a large benefit in both these trials for wearing a stocking, with no major side effects. In 2014, a Canadian group published a trial comparing wearing a compression stocking to wearing a non-compressive stocking. The rates of post-thrombotic syndrome were identical. The Canadian trial also suggested that only half of patients actually wear stockings, one reason the trial may have shown no difference. The Canadian trial suggested that stockings did not prevent future thrombosis or help leg pain. Whilst United Kingdom National Institute for Health and Care Excellence (NICE) recommendations are to avoid stockings after deep vein thrombosis, European recommendations are to still wear them. The contradictory results of these three trials have led us to design the CHAPS trial.

The aim of CHAPS is to confirm whether there is a real benefit of wearing stockings in addition to the standard treatment for deep vein thrombosis, which is blood thinning medication.

Adults with a first deep vein thrombosis can join the trial. They will be randomly allocated to receive either blood thinning medication, or blood thinning medication and an additional compression stocking. This is a tight, custom fitted stocking that they will be asked to wear whilst they are awake as much as possible for between 6-30 months. Patients will be aware of which group they are in, but will be asked not to wear the stocking when they come for their assessment. This keeps the researchers impartial.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2019-09-19
• Study First Submitted QC: 2019-09-23
• Study First Posted: 2019-09-25
• Study Start: 2020-03-05
• Primary Completion: 2022-12-31
• Study Completion: 2022-12-31
• Status Verified: 2023-07
• Results First Submitted: 2023-07-21
• Results First Submitted QC: 2023-07-21
• Last Update Submitted: 2023-07-21
• Results First Posted: 2024-03-07
• Last Update Posted: 2024-03-07

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 152

Inclusion Criteria

• Symptomatic presentation of first deep vein thrombosis, <2 weeks from diagnosis
• Imaging confirmed, lower limb deep vein thrombosis (popliteal, femoral, iliac or combination)
• Ability to give informed consent
• Age 18 or over

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Exclusion Criteria

• Life expectancy < 2 years
• Contraindication to wearing graduated compression stockings
• Previously intolerant of or already wearing graduated compression stockings for more than 1 month.
• Ankle brachial pressure index (ABPI) <0.8 or pedal pulses absent
• Bilateral deep vein thrombosis
• Previous chronic venous insufficiency (patients with existing chronic skin changes or ulceration, defined as C4,5,6 by Clinical Etiological Anatomical Pathophysiological (CEAP) classification)
• Pre-existing post thrombotic syndrome, significant leg pain (e.g. knee arthritis, spinal claudication) or oedema (e.g. lymphoedema).
• Newly diagnosed cancer, metastatic cancer, or cancer undergoing active treatment or palliation
• Contraindication to anticoagulation
• Known allergy to fabric in compression stockings

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Graduated compression stocking and standard clinical care	Graduated compression stocking	A graduated compression stocking and the standard clinical care (anticoagulation)

Primary Outcome Measures

Name	Time	Method
Incidence of Post Thrombotic Syndrome (PTS)	30 months	Measured using the validated Villalta criteria

Secondary Outcome Measures

Name	Time	Method
Employment Status	30 months	Change in number of days working from baseline
Cost-effectiveness of Stocking Prescription	30 months	Incremental cost-effectiveness ratio (ICER) from the EQ-5D questionnaire, with appropriate sensitivity analysis
Venous Ulceration Incidence	30 months	Measured using the validated Villalta criteria
Change in Disease-specific and Generic Quality of Life	18 months	Measured using EuroQoL EQ5D scale (European Quality of Life 5D instrument for measuring generic health status) . A health index on a score of 0 to 1 and the participants' self-rated health on a vertical score of zero to 100. Higher scores indicate better quality of life.
The Proportion of Participants Who Are Adherent to Stockings and Anticoagulants	30 months	Patient self-report - at six months median follow up, the criteria for continuing CHAPS is equal to or over 70% of participants wearing stockings (monthly self-reported patient adherence questionnaire) for equal to or over 4 days per week in the intervention arm, along with a documented reorder of stockings within the last 6 months.

Trial Locations

Locations (12)

Imperial College Healthcare NHS Trust; 🇬🇧 London, United Kingdom

Hampshire Hospitals NHS Foundation Trust; 🇬🇧 Basingstoke, United Kingdom

Basildon and Thurrock University Hospitals NHS Foundation Trust; 🇬🇧 Basildon, United Kingdom

University Hospitals Birmingham NHS Foundation Trust; 🇬🇧 Birmingham, United Kingdom

Kings College Hospital NHS Foundation Trust; 🇬🇧 London, United Kingdom

London North West University Healthcare NHS Trust; 🇬🇧 London, United Kingdom

East Cheshire NHS Trust; 🇬🇧 Macclesfield, United Kingdom

The Newcastle Upon Tyne Hospitals NHS Foundation Trust; 🇬🇧 Newcastle, United Kingdom

Barking, Havering and Redbridge University Hospitals NHS Trust; 🇬🇧 Romford, United Kingdom

Salisbury Hospital NHS Foundation Trust; 🇬🇧 Salisbury, United Kingdom

Guy's and St Thomas' NHS Foundation Trust; 🇬🇧 London, United Kingdom

Royal Free London NHS Foundation Trust; 🇬🇧 London, United Kingdom