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Ultrasound Guided Versus Landmark Guided Small & Medium Joint Arthrocentesis

Ultrasound Guided Versus Landmark Guided Small & Medium Joint Arthrocentesis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03327584
Enrollment
30
Registered
2017-10-31
Start date
2017-01-01
Completion date
2019-12-31
Last updated
2020-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Effusion Joint

Brief summary

Arthrocentesis is the removal of synovial fluid for analysis of pathologic processes. Small & medium joint arthrocentesis will be defined as the following joints: elbow, wrist, finger, ankle and toe. Ultrasound (US) and landmark (LM) small & medium joint arthrocentesis are both performed within the clinical setting. Both techniques are considered standard of care. Selection of which technique to use is dependent upon the physician's preference. There is currently limited data comparing the two methods. The investigators hope to determine if one modality is more effective in terms of success rate, number of attempts, and time to complete the procedure.

Detailed description

Patients presenting to the Emergency Department who are 18 years old or older, who do not belong to a vulnerable group, requiring small or medium joint arthrocentesis will be included in this trial. The investigators will randomize each patient into LM vs US. Data collected will include number of attempts to tap the joint, success rate, and time for procedure to be completed. The arthrocentesis will be performed by PGY-3 residents only. A 21 gauge needle will be used for the arthrocentesis.

Interventions

Athrocentesis

Sponsors

Temple University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* All patients who require an arthrocentesis of a small and/or medium joint (defined previously)

Exclusion criteria

* Coagulopathic patients * Patients on anticoagulants * Patients with cellulitis overlying the joint. * Patients with artificial joints * Adults Unable to Consent * Vulnerable Populations

Design outcomes

Primary

MeasureTime frameDescription
Superiority of Method of arthrocentesis1 dayNumber of attempts until successful arthrocentesis

Secondary

MeasureTime frameDescription
Success of method1 dayCompletion of arthrocentesis after three attempts

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026