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A clinical trial to study the effects of a combination of trypsin-chymotrypsin enzymes and diclofenac in comparison to diclofenac alone in patients with soft tissue injuries.

Phase 3
Completed
Registration Number
CTRI/2009/091/000813
Lead Sponsor
Elder Pharmaceuticals Ltd.,C-9, Dalia Industrial Estate, Veera Desai Road, Off New Link Road,Andheri (W), Mumbai ? 53.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)Adult patients aged between 18 and 65 years with soft tissue injuries like sprains, strains, stress injuries, ecchymosis, hematomas and lacerations seen within 24 hours of the injury
2)Patients aged between 18 and 65 years.
3)Patients who have given their written informed consent
4)Patients of childbearing years who are using appropriate contraceptive methods for 3 weeks prior to the study and throughout the duration of the study.
The following patients may also be included:
1. Clean Lacerated Wounds (non infected) requiring suturing.
2.Patients with healed fractures more than 3 months old

Exclusion Criteria

1)Any long standing/ chronic inflammatory condition like Rheumatoid Arthritis, Osteoarthritis or Spondylitis where the patient has been on long term NSAIDs, Anti-Inflammatory drugs or Analgesics.
2)Infected wounds, Tissue abscesses and Cellulitis
3)Patients with Fracture if less than 3 months old.
4)Post operative cases
5)Patients who have Diabetes/ Raised Blood Sugar
6)Pregnant or breast-feeding women.
7)Patients who are simultaneously participating in another clinical trial with an unlicensed drug or who have done so within a one month period.
8)Patients with a known hypersensitivity to TC or Diclofenac

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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