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Compression Hosiery to Avoid Post-Thrombotic Syndrome (CHAPS)

Primary Purpose

Deep Vein Thrombosis, Deep Vein Thrombosis Leg, Post Thrombotic Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Graduated compression stocking
Sponsored by
Imperial College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Deep Vein Thrombosis focused on measuring Deep Vein Thrombosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

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

Sites / Locations

  • Basildon and Thurrock University Hospitals NHS Foundation TrustRecruiting
  • Hampshire Hospitals NHS Foundation TrustRecruiting
  • University Hospitals Birmingham NHS Foundation TrustRecruiting
  • Imperial College Healthcare NHS TrustRecruiting
  • Guy's and St Thomas' NHS Foundation TrustRecruiting
  • Kings College Hospital NHS Foundation TrustRecruiting
  • London North West University Healthcare NHS TrustRecruiting
  • Royal Free London NHS Foundation TrustRecruiting
  • East Cheshire NHS TrustRecruiting
  • The Newcastle Upon Tyne Hospitals NHS Foundation TrustRecruiting
  • Barking, Havering and Redbridge University Hospitals NHS TrustRecruiting
  • Salisbury Hospital NHS Foundation TrustRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard clinical care

Graduated compression stocking and standard clinical care

Arm Description

Standard clinical care (anticoagulation) with no graduated compression stocking

A graduated compression stocking and the standard clinical care (anticoagulation)

Outcomes

Primary Outcome Measures

Incidence of Post Thrombotic Syndrome (PTS)
Measured using the validated Villalta criteria

Secondary Outcome Measures

Venous ulceration incidence
Measured using the validated Villalta criteria
Employment status
Change in number of days working from baseline
Change in disease-specific and generic quality of life
Measured using VEINES-QoL scale (instrument to measure quality of life in deep venous thrombosis). Two summary scores can be computed. The VEINES-QOL summary score (25 items) provides an estimate of the overall impact of deep venous thrombosis on the patient's quality of life. The VEINES-Sym summary score (10 items) measures symptom severity. Higher scores indicate better outcomes.
Change in disease-specific and generic quality of life
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
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.
Cost-effectiveness of stocking prescription
Incremental cost-effectiveness ratio (ICER) from the EQ-5D questionnaire, with appropriate sensitivity analysis

Full Information

First Posted
September 19, 2019
Last Updated
September 7, 2021
Sponsor
Imperial College London
Collaborators
University of Edinburgh, Universidad de Granada, University College, London, University of Manchester
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1. Study Identification

Unique Protocol Identification Number
NCT04103112
Brief Title
Compression Hosiery to Avoid Post-Thrombotic Syndrome
Acronym
CHAPS
Official Title
Compression Hosiery to Avoid Post-Thrombotic Syndrome (CHAPS)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 5, 2020 (Actual)
Primary Completion Date
July 31, 2022 (Anticipated)
Study Completion Date
January 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London
Collaborators
University of Edinburgh, Universidad de Granada, University College, London, University of Manchester

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis, Deep Vein Thrombosis Leg, Post Thrombotic Syndrome
Keywords
Deep Vein Thrombosis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
An independent researcher at each site will perform leg assessments blind to participant allocation. This researcher will not have been involved in recruitment, stocking provision, adherence monitoring or behavioural interventions. Participants will be encouraged to remove their stockings on the day prior to their clinic visit, they will be asked not to discuss the stockings with the independent assessor. Blinding will be assessed by asking the assessors whether the patient attended study visits wearing a stocking, and whether the patient made it known that they had been wearing a stocking or not.
Allocation
Randomized
Enrollment
864 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard clinical care
Arm Type
No Intervention
Arm Description
Standard clinical care (anticoagulation) with no graduated compression stocking
Arm Title
Graduated compression stocking and standard clinical care
Arm Type
Experimental
Arm Description
A graduated compression stocking and the standard clinical care (anticoagulation)
Intervention Type
Device
Intervention Name(s)
Graduated compression stocking
Intervention Description
Compression stockings have been used safely in the UK for about 50 years. They contain an elastic fibre designed to fit tightly around the legs. These specialist stockings are tighter around the ankle, with the level of compression gradually decreasing up the garment. The pressure created by the stockings helps blood flow up the leg, allowing blood to flow freely to the heart and not pool in the leg which can result in pain and swelling.
Primary Outcome Measure Information:
Title
Incidence of Post Thrombotic Syndrome (PTS)
Description
Measured using the validated Villalta criteria
Time Frame
30 months
Secondary Outcome Measure Information:
Title
Venous ulceration incidence
Description
Measured using the validated Villalta criteria
Time Frame
30 months
Title
Employment status
Description
Change in number of days working from baseline
Time Frame
30 months
Title
Change in disease-specific and generic quality of life
Description
Measured using VEINES-QoL scale (instrument to measure quality of life in deep venous thrombosis). Two summary scores can be computed. The VEINES-QOL summary score (25 items) provides an estimate of the overall impact of deep venous thrombosis on the patient's quality of life. The VEINES-Sym summary score (10 items) measures symptom severity. Higher scores indicate better outcomes.
Time Frame
18 months
Title
Change in disease-specific and generic quality of life
Description
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.
Time Frame
18 months
Title
The proportion of participants who are adherent to stockings and anticoagulants
Description
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.
Time Frame
30 months
Title
Cost-effectiveness of stocking prescription
Description
Incremental cost-effectiveness ratio (ICER) from the EQ-5D questionnaire, with appropriate sensitivity analysis
Time Frame
30 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rebecca Lawton
Phone
0203 311 5204
Email
r.lawton@imperial.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Laura Burgess
Phone
0203311520
Email
l.burgess@imperial.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alun H Davies
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Basildon and Thurrock University Hospitals NHS Foundation Trust
City
Basildon
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shiva Dindyal
Email
shiva.dindyal@btuh.nhs.uk
First Name & Middle Initial & Last Name & Degree
Shiva Dindyal
Facility Name
Hampshire Hospitals NHS Foundation Trust
City
Basingstoke
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tamara Everington
Email
tamara.everington@hhft.nhs.uk
First Name & Middle Initial & Last Name & Degree
Tamara Everington
Facility Name
University Hospitals Birmingham NHS Foundation Trust
City
Birmingham
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrew Bradbury
Email
andrew.bradbury@btinternet.com
First Name & Middle Initial & Last Name & Degree
Andrew Bradbury
Facility Name
Imperial College Healthcare NHS Trust
City
London
ZIP/Postal Code
W68RF
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alun Davies
Email
a.h.davies@imperial.ac.uk
First Name & Middle Initial & Last Name & Degree
Alun H Davies
Facility Name
Guy's and St Thomas' NHS Foundation Trust
City
London
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Beverley Hunt
Email
beverley.hunt@gstt.nhs.uk
First Name & Middle Initial & Last Name & Degree
Beverley Hunt
Facility Name
Kings College Hospital NHS Foundation Trust
City
London
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roopen Arya
Email
Roopen.arya@kcl.ac.uk
First Name & Middle Initial & Last Name & Degree
Roopen Arya
Facility Name
London North West University Healthcare NHS Trust
City
London
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sophie Renton
Email
Sophie.renton@nwlh.nhs.uk
First Name & Middle Initial & Last Name & Degree
Sophie Renton
Facility Name
Royal Free London NHS Foundation Trust
City
London
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anja Drebes
Email
a.drebes@nhs.net
First Name & Middle Initial & Last Name & Degree
Anja Drebes
Facility Name
East Cheshire NHS Trust
City
Macclesfield
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Imran Ansari
Email
imran.ansari1@nhs.net
First Name & Middle Initial & Last Name & Degree
Imran Ansari
Facility Name
The Newcastle Upon Tyne Hospitals NHS Foundation Trust
City
Newcastle
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gerry Stansby
Email
g.stansby@nuth.nhs.uk
First Name & Middle Initial & Last Name & Degree
Gerry Stansby
Facility Name
Barking, Havering and Redbridge University Hospitals NHS Trust
City
Romford
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Claudia Boshier
Email
claudia.boshier@nhs.net
First Name & Middle Initial & Last Name & Degree
Claudia Boshier
Facility Name
Salisbury Hospital NHS Foundation Trust
City
Salisbury
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jonathan Cullis
Email
jonathan.cullis@nhs.net
First Name & Middle Initial & Last Name & Degree
Jonathan Cullis

12. IPD Sharing Statement

Plan to Share IPD
No

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Compression Hosiery to Avoid Post-Thrombotic Syndrome

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