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Intermittent Claudication clinical trials

View clinical trials related to Intermittent Claudication.

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NCT ID: NCT04058171 Completed - Low Back Pain Clinical Trials

Validation of a Treadmill Walking Test to Discriminate Neurogenic Claudication From Vascular Claudication

Start date: May 1, 2018
Phase:
Study type: Observational

The first aim of this study was to elaborate and validate a treadmill walking test that would help discriminate between neurogenic claudication from vascular claudication. The second objective of this study is to determine if the treadmill walking test can discriminate spinal stenosis from low back pain with radiating pain in lower limb.

NCT ID: NCT04043546 Completed - Clinical trials for Peripheral Artery Disease

Observational Feasibility Study of Home-based Training With Therabands in PAD-patients

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

The study is an observational feasibility study to evaluate the feasibility of a combined aerobic+resistance training program in patients with IC.

NCT ID: NCT03898570 Completed - Clinical trials for Cardiovascular Diseases

Distributed Registry

Start date: April 1, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to test if a patient can be directly connected to a quality assurance (QA) database, traditionally known as a registry. Patient-reported outcomes (PRO) data will be entered into the database directly from a patient's mobile phone from their index procedure for 12 months. The investigators hope this study to be a "proof of concept" for such a distributed registry and evaluate 1) consistency of data acquisition, 2) engagement of patients, 3) overall value of patient-reported outcomes to enhance long term follow up.

NCT ID: NCT03864666 Completed - Clinical trials for Intermittent Claudication

Bioequivalence Study of Once Daily PMR Compared to Twice Daily Cilostazol IR Tablets in Healthy Volunteers

Start date: February 11, 2019
Phase: Phase 1
Study type: Interventional

The study is designed to evaluate the bioequivalence and the within-subject variability between the test formulation of extended-release tablet of cilostazol (PMR) administered once daily and the reference formulation of immediate-release tablet of cilostazol (Cilostazol) administered twice-daily in normal healthy male and female subjects under fasting conditions.

NCT ID: NCT03863067 Completed - Clinical trials for Spinal Stenosis, Lumbar Region, With Neurogenic Claudication

Clinical Effectiveness, Security And Radiological Changes In Epiduroscopy For Lumbar Stenosis

Start date: October 15, 2018
Phase: N/A
Study type: Interventional

It will be done a prospective Study involving 38 patients with lumbar stenosis. A magnetic resonance (MR) imaging study and a electromyographic study will be done previously and 3 months after the epiduroscopy to confirm radiologic or neurophysiological changes. During the technic it will be used different instruments, an endoscope developed for its use in the epidural space (Resascope), a Fogarty balloon (Resaloon) to dilate the space near the epidural recess where it will be try to decrease the ligamentum flavum using the Resaflex, an instrument with Quantum Molecular Resonance for tissue coablation, in order to get less symptomatic lumbar stenosis. The investigators will compare qualitative and quantitative variables at baseline and 1, 3, 6, ant 12 months after the epiduroscopy.

NCT ID: NCT03640676 Completed - Clinical trials for Peripheral Arterial Disease

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

Start date: January 14, 2019
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT03590769 Completed - Clinical trials for Peripheral Arterial Disease

Arterial Imaging of Inflammation and Resolution After Endovascular Surgery

AIIRES
Start date: June 1, 2017
Phase: Phase 1
Study type: Interventional

This study evaluates the local inflammatory and resolution response of patients undergoing peripheral vascular intervention like an angioplasty of the superficial femoral artery (SFA) or popliteal artery, or stenting of the iliac artery or SFA, through the use of Positron emission tomography-magnetic resonance imaging (PET/MRI). PET/MRI will be performed prior to intervention, one day and one week after intervention.

NCT ID: NCT03564080 Completed - Clinical trials for Coronary Artery Disease

Assessing the Feasibility of Including Patients With Peripheral Artery Disease in to an Established Cardiac Rehabilitation Service.

Start date: July 18, 2018
Phase: N/A
Study type: Interventional

This study will investigate if patients with peripheral artery disease (PAD) can be successfully incorporated into an already existing Cardiac Rehabilitation programme. One group of PAD patients will exercise as a group, and the other group will exercise alongside patients with coronary artery disease (CAD).

NCT ID: NCT03547817 Completed - Clinical trials for Peripheral Artery Disease

Intermittent Negative Pressure to Improve Blood Flow in Patients With Peripheral Artery Disease: Optimal Pulse Pressure Regime

Start date: May 15, 2018
Phase: N/A
Study type: Interventional

Recent studies have shown that applying intermittent negative pressure (INP) with short negative pressure (-40 mmHg) pulses to the lower extremities increase arterial blood flow velocity and skin blood flow. However, the optimal magnitude of negative pressure to improve blood flow is not known, and needs further investigation. Peripheral arterial blood flow velocity, skin blood flow and skin temperature in the foot will be recorded at different levels of oscillating negative pressure to identify a pressure range which is practically, while at the same time induce clinically relevant changes in blood flow parameters. Heart rate and blood pressure will be recorded to monitor the effects on the central circulation.

NCT ID: NCT03511157 Completed - Clinical trials for Peripheral Arterial Disease

Ischemic Preconditioning Claudication Study

Start date: June 14, 2018
Phase: N/A
Study type: Interventional

This study proposes ischemic preconditioning (IPC) as a novel intervention to improve walking distance in patients with intermittent claudication.