Carpal Tunnel Syndrome Clinical Trial
Official title:
Does Adding Lidocaine to Corticosteroid Injections Reduce Pain Intensity in Hand Surgery
Verified date | December 2023 |
Source | University of Texas at Austin |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study was to determine whether adding Lidocaine to Corticosteroid injections reduce pain intensity in hand surgery.
Status | Completed |
Enrollment | 40 |
Est. completion date | July 1, 2023 |
Est. primary completion date | July 1, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 89 Years |
Eligibility | Inclusion Criteria: - All patients offered a steroid injection in a hand surgeon's office - Aged 18-89 years - English speaking patients - Able to provide informed consent Exclusion criteria: - Non-English/Spanish speakers |
Country | Name | City | State |
---|---|---|---|
United States | University of Texas Health Austin (UTHA) | Austin | Texas |
Lead Sponsor | Collaborator |
---|---|
University of Texas at Austin |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Jefferson scale of patient perception of physician empathy | a 5 item questionnaire of patient's perceived empathy with a range of 5(minimum perceived empathy) to 35( maximum perceived empathy) | through study completion, an average of 6 weeks | |
Primary | Pain intensity during injection | 11-point ordinal scale, with 0 for no pain at all and 10 for worst pain ever | During Injection | |
Primary | Pain Catastrophizing Scale (PCS 4) | A 4 item questionnaire with a range of 0(no pain catastrophizing thoughts) to 16(maximum pain catastrophizing thoughts) | through study completion, an average of 6 weeks | |
Primary | Patient Health Questionnaire (PHQ 2) | a 2 item questionnaire measuring depression symptoms with a range of 0(no depression symptoms
0 to 6(maximum depression symptoms) |
through study completion, an average of 6 weeks | |
Primary | Pain Self-efficacy Questionnaire (PSEQ 2) | A measure of effective coping strategies with a range of 0(no coping strategy) to 12(maximum coping strategies) | through study completion, an average of 6 weeks | |
Secondary | Pain intensity 4 hours after injection | 11-point ordinal scale, with 0 for no pain at all and 10 for worst pain ever | 4 hours after injection | |
Secondary | Pain intensity 5 minutes after injection | 11-point ordinal scale, with 0 for no pain at all and 10 for worst pain ever | 5 minutes after injection |
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