Effect of Standing, Lying and Stockings on Blood Bio-markers (v.1)
Primary Purpose
Chronic Venous Insufficiency
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
SIGVARIS® Class 2 - RAL: 23-32.
Sponsored by
About this trial
This is an interventional basic science trial for Chronic Venous Insufficiency
Eligibility Criteria
Inclusion Criteria:
Patients from the vascular clinic at Ealing Hospital with venous disease
- Venous skin changes including lipodermatosclerosis and pigmentation
- Significant reflux >0.5 seconds on duplex
Volunteers from NHS healthcare workers or the general public
- Absence of venous symptoms
- Freedom from varicose veins or skin changes
Exclusion Criteria:
- Previous treatment for varicose veins on the study leg
- Previous history of deep or superficial vein thrombosis
- Receiving anticoagulation
- Haematological disorders of coagulation or thrombosis
- Pregnancy
- Significant peripheral vascular disease
- Cardiac failure or orthopnoea
- Uncontrolled/active malignancy
- Significant impairment of mobility
- Connective tissue or autoimmune disease
Sites / Locations
- Ealing Hospital, LNWH NHS TrustRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
SIGVARIS®. Class 2 - RAL: 23-32
Arm Description
Graduated elastic compression stockings
Outcomes
Primary Outcome Measures
Number of biomarkers which decrease greater than 20% of the baseline level as a result of the interventions of (i) lying down and with a (ii) stocking
Secondary Outcome Measures
Full Information
NCT ID
NCT02662127
First Posted
January 13, 2016
Last Updated
April 10, 2017
Sponsor
London North West Healthcare NHS Trust
1. Study Identification
Unique Protocol Identification Number
NCT02662127
Brief Title
Effect of Standing, Lying and Stockings on Blood Bio-markers (v.1)
Official Title
Local Endogenous Biomarkers in the Later Stages of Chronic Venous Disease Versus Controls During Gravitational Stress, Prolonged Elevation Recovery and Compression
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Unknown status
Study Start Date
April 2016 (undefined)
Primary Completion Date
July 2017 (Anticipated)
Study Completion Date
July 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
London North West Healthcare NHS Trust
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Venous disease effects 25% of the population and most healthy people experience venous symptoms after standing for too long. The prime function of leg veins is drainage. Failure leads to a condition called chronic venous insufficiency (CVI) with leg pain, heaviness, swelling, varicose veins, ankle skin changes, eczema and occasionally venous ulcers. The aim of the study is to identify blood components (biomarkers) that occur during the damaging phase of standing versus the healing phases of lying recovery and with medical compression stockings. This will be achieved by taking a blood sample from the ankle region at 3 separate visits (days) to the vascular laboratory at Ealing Hospital. The first visit will be after supervised standing for 1 hour. The second after supervised lying and the third standing whilst wearing a medical compression stocking. Healthy volunteers will be compared to patients with advanced CVI.
The potential importance to patients and the public is threefold. Firstly, biomarker profiles will be obtained in each of the 3 states to increase understanding in the cellular mechanisms of damage and recovery. In this way "bad" and "good" biomarkers can be identified. Secondly, drug treatments may develop from this research to adjust biomarkers towards a favourable profile. Thirdly, the success of treating CVI with surgery, venous intervention or compression can be monitored. Whilst it is known that relief of gravitational stress is the treatment for all forms of CVI, the mechanisms of repair and its discrimination from damage have yet to be identified.
Detailed Description
It is well known that graduated elastic compression stockings (GECs) provide a favourable environment by off-setting the damaging effects of dependency, reducing leg oedema, preventing leg ulceration and in symptom relief. On a haemodynamic level, their mechanism of action in augmenting the venous return has been quantified. However, on a molecular level, their action in modulating local endogenous biomarkers towards a favourable profile is poorly understood. This requires further investigation.
Our hypothesis is that there are two types of biomarkers: (i) damaging inflammatory biomarkers which are increased after prolonged gravitational dependency, (i) healing reparative biomarkers which are increased after prolonged elevation recovery. Local venous blood samples draining the area of investigation may be more representative of loco-regional processes than systemic blood samples from the arm.
This is a single centre, collaborative, interventional, controlled, proof-of-concept trial.
The primary aim of this study is to investigate the effect of GEC stockings on modulating biomarkers towards a healing profile.
Planned interventions:
There will be 4 study visits per subject.
Recruitment, patient selection, distribution of information leaflets and consent form, explanation of the demands of the study, claiming of expenses, duplex scanning and visit scheduling.
Formal consent. Blood test. The stage of "damage" will be in the afternoon after standing all morning plus an hour of extra standing in the laboratory.
Blood test. The stage of "healing" will be in the morning after nocturnal sleep plus an hour of extra elevation (20 degrees elevated from supine) in the laboratory.
Blood test. The stage of "treatment" will be from the effects of a class II below knee stocking after standing all morning plus an hour of extra standing in the laboratory.
All venous blood will be taken from the ankle region. The samples will be taken during a gravitational stress, after elevation recovery and after the therapeutic effect of the compression stocking. These specifications must be met with due care and diligence to ensure that the results are meaningful. The samples will be collected in citrated tubes, centrifuged at 5,000 rpm for 10 minutes to achieve platelet poor plasma and stored at -20 degrees for batch analysis.
Proposed biomarkers for quantification:
Radox (IL-2, IL-4, IL-6, IL-8, IL-10, VEGF, IFNγ, TNFα, IL-1α, IL-1β, MCP-1, EGF) and D-dimer.
Matrix metalloproteinases (MMP-1, MMP-2, MMP-3, MMP-7, MMP-8, MMP-9, MMP-10, MMP-12 and MMP-13) and also 4 tissue inhibitors of MMPs (TIMP-1, TIMP-2, TIMP-3 and TIMP-4).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Venous Insufficiency
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
31 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
SIGVARIS®. Class 2 - RAL: 23-32
Arm Type
Experimental
Arm Description
Graduated elastic compression stockings
Intervention Type
Device
Intervention Name(s)
SIGVARIS® Class 2 - RAL: 23-32.
Intervention Description
Below knee graduated elastic compression stocking
Primary Outcome Measure Information:
Title
Number of biomarkers which decrease greater than 20% of the baseline level as a result of the interventions of (i) lying down and with a (ii) stocking
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients from the vascular clinic at Ealing Hospital with venous disease
Venous skin changes including lipodermatosclerosis and pigmentation
Significant reflux >0.5 seconds on duplex
Volunteers from NHS healthcare workers or the general public
Absence of venous symptoms
Freedom from varicose veins or skin changes
Exclusion Criteria:
Previous treatment for varicose veins on the study leg
Previous history of deep or superficial vein thrombosis
Receiving anticoagulation
Haematological disorders of coagulation or thrombosis
Pregnancy
Significant peripheral vascular disease
Cardiac failure or orthopnoea
Uncontrolled/active malignancy
Significant impairment of mobility
Connective tissue or autoimmune disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christopher R Lattimer, MBBS FRCS MS FdIT PhD
Phone
07960502253
Email
c.lattimer9@imperial.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Evi Kalodiki, MD PhD FRCS
Phone
02072627681
Email
e.kalodiki@imperial.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Evi Kalodiki, MD PhD FRCS
Organizational Affiliation
London North West Healthcare NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ealing Hospital, LNWH NHS Trust
City
Ealing
ZIP/Postal Code
UB1 3HW
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chris Dr Lattimer, MD
Email
c.lattimer09@imperial.ac.uk
First Name & Middle Initial & Last Name & Degree
Evi Dr Kalodiki, MD
12. IPD Sharing Statement
Plan to Share IPD
No
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Effect of Standing, Lying and Stockings on Blood Bio-markers (v.1)
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