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NCT05671523
Effect Of Dry Needling On Quality Of Life In Patients With Trigger Fingers
Conditions: Trigger Finger Disorder
Sex: All
Ages: 45 Years – 75 Years
Phase: NA
Enrollment: 40
Sponsor: Cairo University
Summary
This study will be conducted to investigate the effect of dry needling on quality of life in patients with trigger finger
Eligibility Criteria
Inclusion Criteria:40 patients all have trigger fingers lasting at least 4 weeks.Both gender will be includedAge of patients will be 45-75 years oldPain and tenderness at the position of A1 pulley.Nodule palpation, pain, and discomfort when flexing and extending the finger, presence of a clicking sound at the time of flexion or extension of the finger, snapping or locking of the finger.Willing and able to complete study procedures.Exclusion Criteria:Participants with diabetes mellitus.History of trauma, and rheumatoid arthritis.Dialysis treatment.fingers with a history of local gouty/pyogenic disease.Major hand trauma and fear of needles.Any contraindication for deep dry needling such as anticoagulants, infections, bleeding, or psychotic conditions tumors, calcium deposits, or severe osteoarthritis.
Source: ClinicalTrials.gov (NCT05671523). StuddyBuddy aggregates publicly available trial information.