No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
165 (estimated)
Sponsor
The University of Texas Medical Branch, Galveston · Other
Who this trial is looking for
This trial is looking for patients with arthritis or tendon issues in their hands or arms. Participants will receive corticosteroid injections and experience different types of anesthesia to see which method causes the least pain.
Are You a Good Fit for This Trial?
You may be able to join if
I have been diagnosed with bilateral arthritis or tendon issues.
I consent to participate in the study.
I can complete pain rating scales.
I am 18 years old or older.
You may not be able to join if
I opted out of the study.
I can't give my consent for the study or procedure.
I cannot complete pain rating scales.
I am allergic to triamcinolone acetonide, lidocaine, or bupivicaine.
I do not have a diagnosis of arthritis or tendon issues.
Corticosteroid injections are not indicated for me.
I am under 18 years old.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
This research study aims to evaluate injectional pain at the site of needle insertion for corticosteroid injections (CSI) of the upper extremity depending on different modes of anesthetics. Each individual's perception of pain upon receiving a CSI with two out of three modes of anesthesia (control/no anesthesia, vibrational anesthesia, vapo-coolant anesthesia) will be utilized to compare these var…
This research study aims to evaluate injectional pain at the site of needle insertion for corticosteroid injections (CSI) of the upper extremity depending on different modes of anesthetics. Each individual's perception of pain upon receiving a CSI with two out of three modes of anesthesia (control/no anesthesia, vibrational anesthesia, vapo-coolant anesthesia) will be utilized to compare these variables and determine the method that is associated with the least pain.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Any patient of the Principal Investigator who has clinically diagnosed bilateral arthritis, tendinopathy, arthropathy, or compression neuropathy of the hand, wrist, or elbow where treatment with corticosteroid injection is indicated.
* Participants who voluntarily consent to p…
Inclusion Criteria:
* Any patient of the Principal Investigator who has clinically diagnosed bilateral arthritis, tendinopathy, arthropathy, or compression neuropathy of the hand, wrist, or elbow where treatment with corticosteroid injection is indicated.
* Participants who voluntarily consent to participate in the study and sign consent forms.
* Participants who complete all numeric pain rating scales
* Patients aged ≥ 18 years old
Exclusion Criteria:
* Participants who opt out of the study or withdraw consent
* Participants who are determined to be without capacity to consent to study participation or injection procedure by principal investigator
* Participants with inability to complete numeric pain rating scales
* Participants with known allergies to triamcinolone acetonide, lidocaine, or bupivicaine
* Participants without clinically diagnosed bilateral arthritis, tendinopathy, arthropathy, or compression neuropathy of the hand, wrist, or elbow.
* Participants where treatment with corticosteroid injection is not indicated bilaterally.
* Patients ≤ 18 years old
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