CTRI/2010/091/002947
Completed
Phase 3
A randomized comparative study evaluating the efficacy and tolerability of a 1000 IU/ml topical solution of heparin sodium as compared to a 200 IU/G heparin sodium gel in the management of post infusion superficial thrombophlebitis.
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Post infusion superficial thrombophlebitis.
- Sponsor
- Troikaa Pharmaceuticals Ltd
- Enrollment
- 200
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a)Patients in the age group of 18\-60 years
- •b)Patients of both sexes
- •c)Patients on IV infusion
- •d)Superficial thrombophlebitis Grade 2\-4
Exclusion Criteria
- •a)Patients below 18 years and above 60 years of age
- •b)Patients on anticoagulants
- •c)Pregnant and lactating women
- •d)Patients with any contraindication to heparin
- •e)Mentally retarded patients
- •f)Unwilling patients
- •g)Patients with known hypersensitivity to any component of the formulation
- •h)Patients with grade 1 or 5 phlebitis
- •i)Application of other topical anti\-inflammatory agent.
Outcomes
Primary Outcomes
Not specified
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