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Intermittent Negative Pressure to Improve Blood Flow in Patients With Peripheral Artery Disease: Effects After Long-term Treatment

Primary Purpose

Peripheral Arterial Disease, Intermittent Claudication

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
FlowOx
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Arterial Disease

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Ankle-Brachial Index < 0,9, and intermittent claudication

Exclusion Criteria:

  • Incapable to make an informed consent
  • Inability to perform a treadmill test
  • Inability to independently operate FlowOx
  • Severe heart disease such as unstable angina pectoris, severe heart failure (NYHA IV), severe valve failure
  • Severe COPD

Sites / Locations

  • Department of Surgery, Section of Vascular and Thoracic surgery, Sykehuset Sørlandet
  • Department of Vascular Surgery, Oslo University Hospital, Aker
  • Department of Vascular Surgery, St. Olavs Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Active Comparator

Arm Label

INP -10mmHg

INP -40mmHg

Arm Description

In addition to standard medical treatment, patients will receive treatment with FlowOx, applying intermittent negative pressure of -10mmHg one hour in the morning and one hour in the evening at home for 12 weeks.

In addition to standard medical treatment, patient swill receive treatment with FlowOx, applying intermittent negative pressure of -40mmHg one hour in the morning and one hour in the evening at home for 12 weeks.

Outcomes

Primary Outcome Measures

Change in maximal walking distance
Treadmill test
Change in pain-free walking distance
Treadmill test

Secondary Outcome Measures

Change in serum levels of markers of inflammation and endothelial dysfunction
E-selectin, ICAM-I, IL1, IL-6, IL-8, TNF-alfa, TGF-beta, IL-10
Changes in resting and maximal blood flow
Strain-gauge plethysmography
Changes in Ankle-Brachial Index
Changes in arterial blood flow during application of INP
Ultrasound

Full Information

First Posted
August 14, 2018
Last Updated
February 3, 2020
Sponsor
Oslo University Hospital
Collaborators
Otivio AS
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1. Study Identification

Unique Protocol Identification Number
NCT03640676
Brief Title
Intermittent Negative Pressure to Improve Blood Flow in Patients With Peripheral Artery Disease: Effects After Long-term Treatment
Official Title
Intermittent Negative Pressure to Improve Blood Flow in Patients With Peripheral Artery Disease: Effects After Long-term Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
January 14, 2019 (Actual)
Primary Completion Date
December 23, 2019 (Actual)
Study Completion Date
January 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
Otivio AS

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
Studies have shown that intermittent negative pressure (INP) can induce short-term increase in blood flow in the extremity in patients with peripheral artery disease (PAD). Case reports also have indicated that INP treatment has beneficial hemodynamic and clinical effects in patients with lower limb ischemia and hard to heal leg ulcers. However, the clinical and physiological effects of long-term INP treatment are not well documented and needs further investigation.
Detailed Description
A double-blinded randomized sham-controlled trial. Otivio AS is the developer of FlowOx, a noninvasive CE marked device to increase blood flow to the lower extremity. The device acts as a pressure chamber sealed around the patient's lower leg, applying pulses of intermittent negative pressure and atmospheric pressure. The pressure pulses are generated by a control unit, alternating between removing air from- and venting the pressure chamber. Preliminary tests indicate a significant increase in blood flow to the extremity during INP treatment at -40 mmHg, but a similar increase in blood flow was not detected during treatment INP treatment at -10 mmHg. Hence, treatment with -10 mmHg, may serve as a sham intervention, when evaluating the clinical and physiological effects of long-term INP treatment. All patients will receive best medical treatment including advice for smoking cessation, dietary advice, and advice for physical exercise, and pharmacological treatment with statins and platelet inhibitors. Patients will be randomized into two groups, one group receiving INP treatment with a pressure of -10 mmHg, the other group receiving INP treatment with a pressure of -40 mmHg. Treatment will be conducted by the patient him/herself at home, one hour in the morning and one hour in the evening for 12 weeks. Pain-free- and maximal walking distance, ankle-brachial index, arterial blood flow during application of INP, maximal blood flow, and biomarkers of inflammation and endothelial dysfunction will be registered at baseline and after 12 weeks to evaluate the effects of long-term INP treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease, Intermittent Claudication

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Double-blinded randomized sham-controlled trial
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
INP -10mmHg
Arm Type
Sham Comparator
Arm Description
In addition to standard medical treatment, patients will receive treatment with FlowOx, applying intermittent negative pressure of -10mmHg one hour in the morning and one hour in the evening at home for 12 weeks.
Arm Title
INP -40mmHg
Arm Type
Active Comparator
Arm Description
In addition to standard medical treatment, patient swill receive treatment with FlowOx, applying intermittent negative pressure of -40mmHg one hour in the morning and one hour in the evening at home for 12 weeks.
Intervention Type
Device
Intervention Name(s)
FlowOx
Intervention Description
FlowOx is a CE marked device developed to increase blood flow to the lower extremities. A pressure chamber is sealed around the leg below the knee and is connected to a control unit which induces pulses of 10 sec negative pressure, and 7 sec of atmospheric pressure.
Primary Outcome Measure Information:
Title
Change in maximal walking distance
Description
Treadmill test
Time Frame
At baseline and after 12 weeks of treatment
Title
Change in pain-free walking distance
Description
Treadmill test
Time Frame
At baseline and after 12 weeks of treatment
Secondary Outcome Measure Information:
Title
Change in serum levels of markers of inflammation and endothelial dysfunction
Description
E-selectin, ICAM-I, IL1, IL-6, IL-8, TNF-alfa, TGF-beta, IL-10
Time Frame
At baseline and after 12 weeks
Title
Changes in resting and maximal blood flow
Description
Strain-gauge plethysmography
Time Frame
At baseline and after 12 weeks
Title
Changes in Ankle-Brachial Index
Time Frame
At baseline and after 12 weeks
Title
Changes in arterial blood flow during application of INP
Description
Ultrasound
Time Frame
At baseline and after 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ankle-Brachial Index < 0,9, and intermittent claudication Exclusion Criteria: Incapable to make an informed consent Inability to perform a treadmill test Inability to independently operate FlowOx Severe heart disease such as unstable angina pectoris, severe heart failure (NYHA IV), severe valve failure Severe COPD
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonny Hisdal, PhD
Organizational Affiliation
Deprtment of Vascular Diseases, Oslo University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Surgery, Section of Vascular and Thoracic surgery, Sykehuset Sørlandet
City
Kristiansand
Country
Norway
Facility Name
Department of Vascular Surgery, Oslo University Hospital, Aker
City
Oslo
Country
Norway
Facility Name
Department of Vascular Surgery, St. Olavs Hospital
City
Trondheim
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33985385
Citation
Hoel H, Pettersen EM, Hoiseth LO, Mathiesen I, Seternes A, Seljeflot I, Hisdal J. Effects of intermittent negative pressure treatment on circulating vascular biomarkers in patients with intermittent claudication. Vasc Med. 2021 Oct;26(5):489-496. doi: 10.1177/1358863X211007933. Epub 2021 May 13.
Results Reference
derived

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Intermittent Negative Pressure to Improve Blood Flow in Patients With Peripheral Artery Disease: Effects After Long-term Treatment

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