Clinical Trials/IRCT2012122211841N1

IRCT2012122211841N1

Completed

未知

Comparison of therapeutic effect of low-dose low-molecular-weight heparin (enoxaparin) vs. oral prednisone in treatment of patients with lichen planus

Vice chancellor for Administrative and Financial of Medical School0 sites46 target enrollmentTBD

Conditionslichen planus.lichen planus tropicus

Overview

Phase: 未知
Intervention: Not specified
Conditions: lichen planus.
Sponsor: Vice chancellor for Administrative and Financial of Medical School
Enrollment: 46
Status: Completed
Last Updated: 8 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

8 years ago

Study Type

Interventional

Sex

All

Investigators

Sponsor

Vice chancellor for Administrative and Financial of Medical School

Eligibility Criteria

Inclusion Criteria

•patients with disseminated lichen planus at least 6 months represent to the clinic. Exclusion criteria: 1\. Contraindications of heparin and its derivatives, including: hemostasis, acquired or congenital disorder, the risk of bleeding caused by uncontrolled hypertension, active peptic ulcer, recent cerebrovascular accident, sensitivity to enoxaparin or heparin derivatives; 2\. Chronic liver disease; 3\. Hepatitis B and C; 4\. Contraindications for taking oral prednisone; 5\. Medications that are known to lead to the LP like reaction; 6\. Lichen planus of nails; 7\. Scalp involvement; 8\. Ulcerated mucosal lesions; 9\. Heparin therapy complications such as drug sensitivity, acute bleeding.

Exclusion Criteria

Not provided

Outcomes

Primary Outcomes

Not specified

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