Skip to content

HEPAPAD Study

HEPAPAD Study - HEPAPAD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00016415
Enrollment
150
Registered
2020-01-07
Start date
2018-12-14
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I70.29 I73.9

Interventions

Group 1: Retrospective observation of patients who received LMWH (low molecular weight heparin) in a prophylactic dosage in addition to ASS and Clopidogrel for 4 weeks after blade-PTA (n = 100), 4 wee

Sponsors

LBT Zotz/Klimas
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Peripheral Artery Disease of the AFS or AP, treated by means of blade-PTA; observation period with inclusion of patients 2005 - 2011.

Exclusion criteria

Exclusion criteria: pregnancy

Design outcomes

Primary

MeasureTime frame
Rate of re-PTA/stent or peripheral bypass surgery after index-PTA during the observation period of 5 years (2005-2011).

Secondary

MeasureTime frame
- decreased blood flow by ultrasonography - rate of clinical progression of the PAD (measured by means of decline of the painless walking distance or the Fontaine stage) - association of clinical (arterial hypertension, diabetes, hyperlipidemia, nicotine abuse, BMI, TASC score) and laboratory (fibrinogen, activators of protein C/S, antithrombin, factor VIII, factor V Leiden, prothrombin G20210A, platelet receptor polymorphisms (HPA-1a/b, GPIa807CT), homocysteine, cholesterol, triglycerides, lipoprotein (a)) variables with patency rate in vessels

Countries

Germany

Contacts

Public ContactMichael Edelmann

LBT Zotz/Klimas

edelmann@gefaess-zentrum.com0211-1754660

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026