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Not Yet Recruiting 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.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05671523). StuddyBuddy aggregates publicly available trial information.