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Low-Dose Enoxaparin in Psoriasis

Z

Zagazig University

Status

Not yet enrolling

Conditions

Psoriasis

Treatments

Drug: Subcutaneous Enoxaparin

Study type

Interventional

Funder types

Other

Identifiers

NCT06416566
Enoxaparin in psoriasis

Details and patient eligibility

About

Rationale:

  • Psoriasis is a chronic immune-mediated inflammatory skin disorder where T cells play a fundamental role in its pathogenesis.
  • Low molecular weight heparin has been reported to exert immunomodulatory effect at small doses through inhibition of T cells heparinase enzyme.
  • Low molecular weight heparin may have promising results for treatment of psoriasis.

Research question:

  • Can low molecular weight heparin be used safely for treatment of psoriasis with good outcome?
  • Is enoxaparin inhibitory effect on T cell heparinase enzyme responsible for its beneficial effect?

Hypothesis:

  • Low molecular weight heparin can achieve good results when used at small doses for treatment of psoriasis.
  • Heparin can exert immunomodulatory effect in psoriasis through inhibition of T cell heparinase enzyme.

AIM OF WORK

-The aim of this work is to assess the possible clinical efficacy and safety of low-dose enoxaparin in the treatment of psoriasis and to detect if inhibition of heparinase enzyme might account for its beneficial therapeutic effect.

Objectives:

  • To evaluate safety and efficacy of low molecular weight heparin at small dose for treatment of psoriasis.
  • Contribute to the ongoing efforts to optimize psoriasis management and improve the lives of individuals affected by this chronic condition.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with plaque psoriasis, who met the following criteria will be enrolled.

    1. Age 18 and above.
    2. No systemic (oral, parenteral, photobiological) treatment for psoriasis within the last 2 months.
    3. No topical treatment for psoriasis within the last 2 weeks.

Exclusion criteria

    1. Pregnancy or lactation. 2. Hypersensitivity to heparin and heparin derivatives and a history of heparin-induced thrombocytopenia.

    2. History of bleeding diathesis, uncontrolled hypertension, cerebrovascular accident, peptic ulcer, liver disease and/or abnormal liver function tests or abnormal kidney function tests.

    3. History of major surgery within the last 3 months. 5. A family history of bleeding diathesis, or cerebrovascular accident. 6. Concomitant use of oral anticoagulants, acetylsalicylic acid, or other nonsteroidal anti-inflammatory drugs.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Enoxaparin
Experimental group
Description:
will receive subcutaneous enoxaparin
Treatment:
Drug: Subcutaneous Enoxaparin

Trial contacts and locations

0

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Central trial contact

Nourhan Anis

Data sourced from clinicaltrials.gov

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