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Comparison the effect of acupuncture in treatment of De Quervain’s disease with steroid injection

Comparison the effect of acupuncture treatment with local methylprednisolone acetate injection in De Quervain's tenosynovitis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013012012194N1
Enrollment
30
Registered
2013-02-13
Start date
2013-01-07
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

De Quervain's tenosynovitis. Radial styloid tenosynovitis [de Quervain]

Interventions

Intervention 1: Intervention group (Acupuncture): Sterile needles are inserted perpendicularly into LI-5 , LU-7, LU-9 and also ashi points (points with maximal tenderness) to the depth of 0.5 cun. The
Treatment - Other
Treatment - Drugs
Intervention group (Acupuncture): Sterile needles are inserted perpendicularly into LI-5 , LU-7, LU-9 and also ashi points (points with maximal tenderness) to the depth of 0.5 cun. These points are se
Control group (injection): To inject the sheath around the abductor pollicis longus and extensor pollicis brevis tendons, the insulin needle is inserted 1 cm proximal to the radial styloid process at

Sponsors

Vice chancellor for research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: The patients with clinical diagnosis of De Quervain's tenosynovitis including pain and swelling around styloid process of radius and positive Finkelstein test who have symptoms more than 4 weeks. Exclusion criteria: The patients with acute symptom less than 4 weeks; history of direct trauma or fracture of wrist; previous history of local injection or surgery around styloid process of radius; uncontrolled concomitant disease such as diabetes mellitus or coagulopathy; abnormal findings in blood tests and radiography of wrist.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Prior to the intervention, 2 weeks and 6 weeks after the end of intervention. Method of measurement: Visual Analogue Scale (VAS) score.;Function. Timepoint: Prior to the intervention, 2 weeks and 6 weeks after the end of intervention. Method of measurement: Quick- Disabilities of the Arm, Shoulder and Hand (Q-DASH) score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Alireza Ashraf

Shiraz university of medical sciences

ashrafa@sums.ac.ir+98 71 1231 9040

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026