EUCTR2005-005591-32-GB
Active, not recruiting
Phase 1
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
Derby Hospitals NHS Foundation Trust0 sites20 target enrollmentApril 10, 2006
ConditionsFinger tip injuries
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Finger tip injuries
- Sponsor
- Derby Hospitals NHS Foundation Trust
- Enrollment
- 20
- Status
- Active, not recruiting
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Not specified
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