Expired Study
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Hershey, Pennsylvania 17033


Purpose:

This research is being done to compare pain relief and efficacy of trigger finger injection using a combination of lidocaine/corticosteroid versus corticosteroid injection alone versus corticosteroid/saline combination.


Study summary:

This is a prospective, randomized study comparing pain relief and efficacy of trigger finger injection using a combination of lidocaine/corticosteroid versus corticosteroid injection alone versus corticosteroid/saline combination.


Criteria:

Inclusion Criteria: - Age 18-90 - Male or female (non-pregnant) - Clinically diagnosed trigger digit - Subject is able to provide voluntary, written informed consent - Subject, in the opinion of the clinical investigator, is able to understand the clinical investigation and is willing to perform all study procedures and follow-up visits. Exclusion Criteria: - Age <18 or >90 - Pregnant or lactating women - Non-English speaking individuals - Medication contradictions to lidocaine, corticosteroids and/or saline - Prior injection or surgery on the affected finger - Diagnosis of reflex symptomatic dystrophy (RSD) or complex regional pain syndrome (CRPS) - Open wound


NCT ID:

NCT02421419


Primary Contact:

Principal Investigator
Kenneth Taylor, MD
Milton S. Hershey Medical Center


Backup Contact:

N/A


Location Contact:

Hershey, Pennsylvania 17033
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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