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Effect Of Dry Needling On Quality Of Life In Patients With Trigger Fingers

Sponsored by Cairo University

About this trial

Last updated 2 years ago

Study ID

p.t.REC/012/003924

Status

Completed

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18-75 Years
45 to 75 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 2 years ago

What is this trial about?

This study will be conducted to investigate the effect of dry needling on quality of life in patients with trigger finger

What are the participation requirements?

Yes

Inclusion Criteria

- 40 patients all have trigger fingers lasting at least 4 weeks.

- Both gender will be included

- Age of patients will be 45-75 years old

- Pain 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.

No

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.

Locations

Location

Status