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Efficacy of steroid injection and wrist splint in carpal tunnel syndrome

Comparison efficacy of triamcinolone and wrist splint in severe carpal tunnel syndrome in Pregnancy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012110210799N3
Enrollment
70
Registered
2013-02-12
Start date
2012-11-30
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

Carpal tunnel syndrome. Mononeuropathies of upper limb,Carpal tunnel syndrome

Interventions

Intervention 1: The second group wear wrist splint(product of Iran Odor company) for 8 weeks during nights. Intervention 2: The first group receive 40 mg triamcinolone Acetonide(Triamhexal 40,1 mg
Treatment - Devices
Treatment - Drugs
The second group wear wrist splint(product of Iran Odor company) for 8 weeks during nights.
The first group receive 40 mg triamcinolone Acetonide(Triamhexal 40,1 mg crystalline suspension,intraarticular,manufactured of Holzkirchen factory in Germany)in involved wrist of severe CTS.

Sponsors

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

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria includes women that had paresthesia of hands during pregnancy(pregnancy related carpal tunnel syndrome) and ages between 15 and 49 y/o). Exclusion criteria in this study are diabetes mellitus, collagen vascular disease, renal failure, hypothyroidism, rheumatoid disease, pre-pregnancy carpal tunnel syndrome, positive family history of neuropathy, carpal tunnel surgery and fracture of wrist bones.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of pregnancy related CTS. Timepoint: In start of study and 2 months after intervention. Method of measurement: Clinical examination and electrodiagnostic studies.

Secondary

MeasureTime frame
Pain and numbness of fingers. Timepoint: Before and 2 months after treatment intervention. Method of measurement: Visual analogue scale and electrodiagnostic studies.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHosin Rahimipour

Yasuj University of Medical Sciences

-+98 74 1223 1005

Outcome results

None listed

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