A prospective study to assess the effectiveness of lignocaine versus normal saline in the reduction of pain associated with dressing removal in finger tip injuries
Phase 1
- Conditions
- Finger tip injuries
- Registration Number
- EUCTR2005-005591-32-GB
- Lead Sponsor
- Derby Hospitals NHS Foundation Trust
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
Patients who have sustained a nailbed injury, partial or full amputation of the finger tip
Patients over the age of 16 years
Patients willing to participate in study
Are the trial subjects under 18? yes
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Patients who have previous injury or surgery to the presenting digit
Patients within any other concommitant trial involving analgesics
Patients allergic to lignocaine
Patients who are unable to give consent
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method