IRCT20220625055267N1
Not yet recruiting
Phase 3
Preparation, characterization and clinical evaluation of the effectiveness of a cotton-based topical product in stopping bleeding from the leech therapy wound
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Bleeding from the site of leech therapy.
- Sponsor
- Mashhad University of Medical Sciences
- Enrollment
- 20
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Adults who have leech therapy indication according to the doctor's opinion.
Exclusion Criteria
- •Clinical or laboratory evidence of coagulation disorder (ecchymosis, hematoma, petechiae purpura or disorder in PT, PTT, hemoglobin, platelets, glucose, calcium, urea, creatinine)
- •Patients who take drugs that affect coagulability, including anti\-platelets (aspirin, clopidogrel (Plavix), dipyridamole (Perzantin), ticlopidine (Ticlid), anticoagulants (warfarin, enoxaparin, rivaroxaban, heparin, streptokinase, etc.), blood thinners such as tranexamic acid, vitamin K, aminocaproic acid and statins and oral contraceptives and herbal anticoagulants such as products containing ginger and garlic
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- •Patients with various malignancies
- •Menstruating women
- •Leech therapy in the face area
- •Skin sensitivity to the product
Outcomes
Primary Outcomes
Not specified
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