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Endoveneous Histologic Study

Primary Purpose

Varicose Veins

Status
Withdrawn
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Clarivein
Sponsored by
Rijnstate Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Varicose Veins focused on measuring MOCA, VSM, Clarivein, Histological

Eligibility Criteria

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

Inclusion Criteria:

  1. Elective indication for leg amputation
  2. Peripheral arterial disease
  3. Age > 18 years
  4. Written informed consent

Exclusion Criteria:

  1. Patient is incapable of informed consent
  2. Pregancy and lactation
  3. Previous surgical or endovenous treatment of the greater saphenous vein in the amputed leg
  4. Great saphenous vein is used for bypass surgery
  5. INR > 1.8
  6. ASA 5

Sites / Locations

  • Rijnstate

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Aethoxysklerol clarivein during leg amp

Arm Description

Clarivein treatment with Aethoxysklerol in 5 patients during lower or upper leg amputation

Outcomes

Primary Outcome Measures

Occlusion of the with Clarivein treated vein
Occlusion of the with the Clarivein (Aethoxysklerol) treated vein, check wheter or not treatment was succesfull.
Depth of damage inside and/or outside the venous wall
Depth of damage inside and/or outside the venous wall is to check whether or not the venous wall is damaged due to the Clarivein treatment

Secondary Outcome Measures

Analysis of intraluminal clot / scar
After excision of the treated vein of the amputated leg it will be analysed on intraluminal clot/scar
Morphological changes of the saphenous nerve due to damage of treatment
Analyses of the changes of the saphenous nerve in the treated area (amputated lef) due to the Clarivein treatment.
Perivascular damage resulting from treatment
Analyses of the perivascular damage in the amputated leg as a result of the treatment

Full Information

First Posted
October 13, 2017
Last Updated
November 26, 2018
Sponsor
Rijnstate Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03326219
Brief Title
Endoveneous Histologic Study
Official Title
Histopathological Study of the Vena Saphena Magna After Mechanochemical Endoveneous Ablation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Withdrawn
Why Stopped
Difficulty finding eligible patients
Study Start Date
January 2017 (Actual)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
December 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rijnstate Hospital

4. Oversight

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

5. Study Description

Brief Summary
A new technique, mechanochemical endovenous ablation (MOCA), using the ClariVein ® system is recently developed. To date, histopathological data after mechanochemical endovenous ablation are not known. The aim of this study is the histopathological analysis of venous injury using mechanochemical endovenous ablation.
Detailed Description
Background: Varicose veins are a common problem in the Western world. Epidemiological studies show that one quarter of adults have some form of varicose veins. Women are two to three times more affected than men. The prevalence of varicose veins increases steadily with age and is among the top ten of the complaints that people visit their General Practitioner. The main risk factors are prolonged standing or sitting, pregnancy, gender and age. The symptoms of varicose veins are variable and range from cosmetic complaints to venous ulcers. Stripping of the great saphenous vein(GSV) has been the golden standard for GSV insufficiency for a long time. It is performed under regional or general anesthesia and has a high recurrence rate of 18-40% at 5 years. In addition, the procedure leads to significant postoperative symptoms, especially pain, hematoma and the risk of injury to the saphenous nerve. In recent years, endovenous techniques have been developed for the treatment of primary GSV insufficiency. Particularly laser endovenous ablation (EVLA) and radiofrequency ablation (VNUS) became accepted technologies and are widely applied in practice. These thermal-based techniques have the advantage that the surgery can be performed with local anesthesia. In addition, endovenous techniques cause less hematoma, pain, and have superior cosmetics and earlier resumption of normal activities/work compared to the conventional surgical stripping. Endothermal techniques use heat, which has potential risk to damage surrounding tissues. For this reason, patients are treated with tumiscence anesthesia, requiring multiple punctures around the vein. Most patients experience tumiscence anesthesia as unpleasant. Despite the tumiscence anesthesia, patients may still observe postoperative pain, which may last for weeks. Laser energy is absorbed and converted into intraluminal heat. This process causes steam bubbles, as described by Proebstle. In previous studies, intraluminal and extraluminal temperature measurements were done during endovenous laser ablation. In addition, acute pathological changes after endovenous laser ablation is studied in a recent study. The loss of laser energy was confined to the inner part of the media. No perivascular damage was seen. However, 1% of patients treated with endovenous laser ablation has nerve damage or paresthesias. It suggests that perivascular damage to some extent still exists. The effects of foam sclerosis appear to be limited to the endothelium and tunica media of the vein wall. Pathological changes occur rapidly within the first 2 minutes after treatment. After 30 minutes intimal detachment of the tunica media, and the formation of microthrombi are detected. The addition of a balloon injury of the vessel wall prior to foam sclerosis, results in a higher percentage of endothelial damage. However, in practice, the clinical results of foam sclerosis disappointing. The occlusionrate from 1 to 5 years were 81 and 73% in a recent meta-analysis. A new technique, mechanochemical endovenous ablation (MOCA), using the ClariVein ® system is recently developed. The first studies show that MOCA a safe and effective treatment for varicose veins. This technique uses mechanical damage to the endothelium of the vein wall through a rotating tip of the catheter. At the same time a sclerosans is injected, causing occlusion of the vein. No heating is used in this technique . Tumiscence anesthesia is redundant and complications that occur in thermal endovenous techniques, such as pain, hematoma formation, induration and paresthesias could be reduced. To date, histopathological data after mechanochemical endovenous ablation are not known. Objective of the study: The aim of this study is the histopathological analysis of venous injury using mechanochemical endovenous ablation Study design: The Endovenous Histology study is a histopathological study on the effects of mechanochemical endovenous ablation. The studycentre will be: - Rijnstate Hospital, Arnhem. 5 patients with irreversible tissue damage to the lower extremities based on atherosclerotic peripheral vascular disease will be included in the study Endovenous Histology, after signing informed consent. All patients included, are scheduled for an elective upper or underleg amputation. The preprocedural status will be determined by height, weight, comorbidities, ASA classification, medications, previous vascular surgery and venous duplex of the VSM. Subsequently 5 patients are treated with MOCA of the VSM to the amputation level prior to the amputation under general or spinal anesthesia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Varicose Veins
Keywords
MOCA, VSM, Clarivein, Histological

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Aethoxysklerol clarivein during leg amp
Arm Type
Other
Arm Description
Clarivein treatment with Aethoxysklerol in 5 patients during lower or upper leg amputation
Intervention Type
Procedure
Intervention Name(s)
Clarivein
Intervention Description
The Clarivein technique uses mechanical damage to the endothelium of the vein wall through a rotating tip of the catheter. At the same time a sclerosans is injected, causing occlusion of the vein. No heating is used in this technique .
Primary Outcome Measure Information:
Title
Occlusion of the with Clarivein treated vein
Description
Occlusion of the with the Clarivein (Aethoxysklerol) treated vein, check wheter or not treatment was succesfull.
Time Frame
2 years of inclusion and analyzation
Title
Depth of damage inside and/or outside the venous wall
Description
Depth of damage inside and/or outside the venous wall is to check whether or not the venous wall is damaged due to the Clarivein treatment
Time Frame
2 years of inclusion and analyzation
Secondary Outcome Measure Information:
Title
Analysis of intraluminal clot / scar
Description
After excision of the treated vein of the amputated leg it will be analysed on intraluminal clot/scar
Time Frame
2 years of inclusion and analyzation
Title
Morphological changes of the saphenous nerve due to damage of treatment
Description
Analyses of the changes of the saphenous nerve in the treated area (amputated lef) due to the Clarivein treatment.
Time Frame
2 years of inclusion and analyzation
Title
Perivascular damage resulting from treatment
Description
Analyses of the perivascular damage in the amputated leg as a result of the treatment
Time Frame
2 years of inclusion and analyzation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Elective indication for leg amputation Peripheral arterial disease Age > 18 years Written informed consent Exclusion Criteria: Patient is incapable of informed consent Pregancy and lactation Previous surgical or endovenous treatment of the greater saphenous vein in the amputed leg Great saphenous vein is used for bypass surgery INR > 1.8 ASA 5
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MMPJ Reijnen, MD
Organizational Affiliation
Rijnstate
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rijnstate
City
Arnhem
State/Province
Gelderland
ZIP/Postal Code
68ooTA
Country
Netherlands

12. IPD Sharing Statement

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Endoveneous Histologic Study

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