Peripheral Artery Disease Clinical Trial
Official title:
SHOW-ME PAD (Peripheral Artery Disease)
NCT number | NCT03190382 |
Other study ID # | 17-053 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 24, 2017 |
Est. completion date | April 1, 2024 |
Verified date | May 2024 |
Source | Saint Luke's Health System |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The overall goal of SHOWME-PAD is to make the existing evidence-base on treatment outcomes -focusing on health status outcomes that reflect the patients' perspective - more transparently available to patients and providers, such that more informed, evidence-based shared treatment decisions occur. INTEGRITY-PAD has the potential to radically reorganize care delivery to patients with PAD such that more value for the patient and society will be created.
Status | Completed |
Enrollment | 72 |
Est. completion date | April 1, 2024 |
Est. primary completion date | September 30, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - All race and ethnicity categories, English speaking, men and women - Age =18 years - New onset complaints of PAD symptoms or exacerbation of previous PAD symptoms - The diagnostic enrollment criterion includes a positive result for one of the following - Doppler resting ankle-brachial index (ABI)=0.90 or a significant drop in post exercise ankle pressure of =20 mmHg. - Duplex - CTA - MRA - TCOM - Angiogram Exclusion Criteria: - Non-compressible ankle-brachial index (ABI = 1.30) - A lower limb revascularization procedure in the ipsilateral leg (same leg) where the patient is currently having symptoms in the past year (atherectomy, endarterectomy, bypass surgery, angioplasty) - Peripheral intervention that occurs before the baseline interview - Current episode of critical limb ischemia (ischemic rest pain, ulceration or gangrene) (Fontaine III, IV or Rutherford IV-VI) - Patients with dementia - Patients who are prisoners - Patients who are unable to provide informed consent - Non-English speaking patients |
Country | Name | City | State |
---|---|---|---|
United States | Saint Luke's Hospital of Kansas City | Kansas City | Missouri |
Lead Sponsor | Collaborator |
---|---|
Saint Luke's Health System | Merck Sharp & Dohme LLC |
United States,
de Graaff JC, Ubbink DT, Kools EI, Chamuleau SA, Jacobs MJ. The impact of peripheral and coronary artery disease on health-related quality of life. Ann Vasc Surg. 2002 Jul;16(4):495-500. doi: 10.1007/s10016-001-0121-9. Epub 2002 Jun 27. — View Citation
O'Connor AM. Validation of a decisional conflict scale. Med Decis Making. 1995 Jan-Mar;15(1):25-30. doi: 10.1177/0272989X9501500105. — View Citation
Rooke TW, Hirsch AT, Misra S, Sidawy AN, Beckman JA, Findeiss LK, Golzarian J, Gornik HL, Halperin JL, Jaff MR, Moneta GL, Olin JW, Stanley JC, White CJ, White JV, Zierler RE; Society for Cardiovascular Angiography and Interventions; Society of Interventional Radiology; Society for Vascular Medicine; Society for Vascular Surgery. 2011 ACCF/AHA Focused Update of the Guideline for the Management of Patients With Peripheral Artery Disease (updating the 2005 guideline): a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2011 Nov 1;58(19):2020-45. doi: 10.1016/j.jacc.2011.08.023. Epub 2011 Oct 6. No abstract available. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Decisional Conflict | The primary outcome of this study will be decisional conflict as measured by the Decisional Conflict Scale. | 6 months |
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