Critical Limb Ischemia Clinical Trial
— PROVENCEOfficial title:
Prospective Observation Study of Patient Outcome and Cost Effectiveness of Interventions for Critical Ischemia
NCT number | NCT01794494 |
Other study ID # | PROVENCE-1 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | November 2011 |
Est. completion date | January 2019 |
Verified date | April 2023 |
Source | Sahlgrenska University Hospital, Sweden |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
Severe atherosclerosis in the leg arteries is termed critical limb ischemia (CLI). This condition gives great suffering for the patients in terms of pain, wounds and often developing gangrene. Untreated, the condition has a high risk of amputation. In Sweden, the majority of the patients are investigated and evaluated for treatment. Treatment is carried out either by traditional open bypass surgery or balloon dilatation technology (endovascular treatment). The latter method is still under development, and studies have shown that the treatment has less local and systemic complications than bypass surgery. It is also shown that the method has a limitation in that the treatment effect is less durable. What is the role of minimally invasive technologies should have in the future is unclear, mainly due to its efficiency and cost-effectiveness compared with bypass surgery are not evaluated. In a prospective observational study we intend study the effectiveness, cost-effectiveness and impact on quality of life in patients undergoing treatment for critical CLI with bypass surgery or endovascular treatment in Västra Götaland Region (VGR). All patients over a period of two years, which undergo treatment for CLI with either of the two methods will be included in the study. Patients will be followed up with regard to the clinical efficacy and health-related quality of life after treatment at, respectively one, 12 and 24 and 60 months. Cumulative care costs are calculated and estimates of cost are made. This study aims to increase knowledge about the role of endovascular treatment of CLI shall have in the future.
Status | Completed |
Enrollment | 190 |
Est. completion date | January 2019 |
Est. primary completion date | January 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - patients with CLI due to arterial occlusion of the superficial femoral artery and/or the popliteal artery being considered for bypass surgery or SAP at any of the four vascular surgical units in VGR. Exclusion Criteria: - patients with CLI due to arterial occlusion of the aorto-iliac arterial segment or distal to the politeal segment. - Patients with inability to understand patientinformation and informed concens. |
Country | Name | City | State |
---|---|---|---|
Sweden | Department of vascular surgery, Sahlgrenska University Hospital | Gothenborg |
Lead Sponsor | Collaborator |
---|---|
Sahlgrenska University Hospital, Sweden | Vastra Gotaland Region |
Sweden,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Rate of re-intervention | Primary patency: Freedom from occlusion of bypass-graft or endovacular treated arterial segment and freedom of restenosis that need intervention in bypass-graft or endovascular treated arterial segment.
Secondary patency:Freedom from occlusion of bypass-graft or endovacular treated arterial segment. Treated for restenosis in bypass-graft or endovascular treated arterial segment. |
2 years | |
Other | Health related quality of life | Health related quality of life measured by VASCUQOL. VascuQol consists of 25 items, subdivided into five domains. Each question has a seven-point response scale. The responses are averaged to give an overall and a domain score ranging from one (worst Health Related Quality of Life, HRQoL) to seven (best HRQoL). | 2 years | |
Other | Health related quality of life | Health related quality of life measured by EQ-5D-3L. EuroQol- 5 dimensions (EQ-5D-3L) consists of 5 items, subdivided into five domains. Each question has a three-point response scale. The score is used to calculate an index between 0 (worst HR) to 1 (best HRQoL). | 2 years | |
Other | Cost effectiveness | Cumulative health care costs in dollars | 2 years | |
Primary | Amputation-free survival | Freedom of death and amputation during the study | 2 years | |
Secondary | Change in Rutherford scale | Change in Rutherford scale from baseline:International established scoring system 0-6 for grading of lower limb ischemia. | 2 Years |
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