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Steroid Injection Treatment of Carpal Tunnel Syndrome

Primary Purpose

Carpal Tunnel Syndrome

Status
Completed
Phase
Phase 2
Locations
Sweden
Study Type
Interventional
Intervention
Methylprednisolone 40 mg
Methylprednisolone 80 mg
Sodium chloride
Sponsored by
Region Skane
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carpal Tunnel Syndrome

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary, idiopathic CTS
  • Age 18-70 years, either gender
  • Symptom duration of at least 3 months and inadequate response to wrist splint
  • Symptoms of classic or probable CTS according to the diagnostic criteria in Katz hand diagram
  • Nerve conduction studies showing median neuropathy at the wrist and no other abnormalities or, in the absence of abnormal nerve conduction study results, 2 surgeons should independently diagnose the patient with CTS.
  • Scheduled for carpal tunnel release (ie, symptom severity indicating need for surgery)exclusion criteria

Exclusion Criteria:

  • Previous steroid injection for CTS in the same wrist
  • Inflammatory joint disease, diabetes mellitus· Vibration-induced neuropathy, polyneuropathy
  • Pregnancy
  • Trauma to the affected hand in the previous year
  • Previous CTS surgery in the affected hand
  • Inability to complete questionnaires due to language problem or cognitive disorder
  • Severe medical illness
  • Known abuse of drugs and/or alcohol

Sites / Locations

  • Ortopediska kliniken, sjukvårdsorganisationen Hässleholm/CSK

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

A

B

C

Arm Description

Outcomes

Primary Outcome Measures

The CTS symptom severity score after treatment.
Rate of surgery

Secondary Outcome Measures

The CTS symptom severity score after treatment
Time to surgery
QuickDASH score
SF-6D score
Patient satisfaction with the results of treatment (VAS scale)
Registration of adverse events

Full Information

First Posted
December 10, 2008
Last Updated
April 3, 2012
Sponsor
Region Skane
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1. Study Identification

Unique Protocol Identification Number
NCT00806871
Brief Title
Steroid Injection Treatment of Carpal Tunnel Syndrome
Official Title
Local Steroid Injection in the Treatment of Idiopathic Carpal Tunnel Syndrome: A Randomized Double-blind Placebo-controlled Trial Among Patients Planned for Surgical Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
March 2011
Overall Recruitment Status
Completed
Study Start Date
November 2008 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Region Skane

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to assess the efficacy of injecting steroid into the carpal tunnel in relieving symptoms of carpal tunnel syndrome for at least 1 year with outcomes measured with patient evaluated symptoms score.Out of the patients referred by primary care, those with a clinical diagnosis of CTS who have tried wrist splint and whose symptom severity is judged by the examining surgeon to warrant surgery are offered to be put on the waiting list for carpal tunnel release. This means a waiting time of approximately 3 months. Patients who give informed consent will be asked to attend the outpatient clinic for a physical examination followed by allocation to one of the three trial groups. Immediately following the allocation the patients will receive the assigned treatment.
Detailed Description
www.biomedcentral.com/1471-2474/11/76

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carpal Tunnel Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
112 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Active Comparator
Arm Title
B
Arm Type
Active Comparator
Arm Title
C
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone 40 mg
Other Intervention Name(s)
Depo-medrol
Intervention Description
Depo-medrol 40 mg , suspension, injection in the carpal tunnel, one time use 1 ml 40 mg Methylprednisolone + 1 ml 10mg Lidocaine + 1 ml saline
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone 80 mg
Other Intervention Name(s)
Depo-medrol
Intervention Description
Depo-medrol 80 mg , suspension, injection in the carpal tunnel, one time use. 2 ml 80mg Methylprednisolone + 1 ml 10mg Lidocaine
Intervention Type
Drug
Intervention Name(s)
Sodium chloride
Other Intervention Name(s)
Saline, NaCl
Intervention Description
Saline solution 0,9%, injection in the carpal tunnel, one time use 1 ml 10 mg Lidocaine + 2 ml saline
Primary Outcome Measure Information:
Title
The CTS symptom severity score after treatment.
Time Frame
10 weeks
Title
Rate of surgery
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
The CTS symptom severity score after treatment
Time Frame
52 weeks
Title
Time to surgery
Time Frame
52 weeks
Title
QuickDASH score
Time Frame
52 weeks
Title
SF-6D score
Time Frame
52 weeks
Title
Patient satisfaction with the results of treatment (VAS scale)
Time Frame
52 weeks
Title
Registration of adverse events
Time Frame
24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary, idiopathic CTS Age 18-70 years, either gender Symptom duration of at least 3 months and inadequate response to wrist splint Symptoms of classic or probable CTS according to the diagnostic criteria in Katz hand diagram Nerve conduction studies showing median neuropathy at the wrist and no other abnormalities or, in the absence of abnormal nerve conduction study results, 2 surgeons should independently diagnose the patient with CTS. Scheduled for carpal tunnel release (ie, symptom severity indicating need for surgery)exclusion criteria Exclusion Criteria: Previous steroid injection for CTS in the same wrist Inflammatory joint disease, diabetes mellitus· Vibration-induced neuropathy, polyneuropathy Pregnancy Trauma to the affected hand in the previous year Previous CTS surgery in the affected hand Inability to complete questionnaires due to language problem or cognitive disorder Severe medical illness Known abuse of drugs and/or alcohol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isam Atroshi, MD, PhD
Organizational Affiliation
Lund university, department of clinical sciences, Hässleholm hospital, department of orthopedics
Official's Role
Study Chair
Facility Information:
Facility Name
Ortopediska kliniken, sjukvårdsorganisationen Hässleholm/CSK
City
Hässleholm
ZIP/Postal Code
281 25
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
10411196
Citation
Atroshi I, Gummesson C, Johnsson R, Ornstein E, Ranstam J, Rosen I. Prevalence of carpal tunnel syndrome in a general population. JAMA. 1999 Jul 14;282(2):153-8. doi: 10.1001/jama.282.2.153.
Results Reference
background
PubMed Identifier
12877853
Citation
Atroshi I, Gummesson C, Johnsson R, McCabe SJ, Ornstein E. Severe carpal tunnel syndrome potentially needing surgical treatment in a general population. J Hand Surg Am. 2003 Jul;28(4):639-44. doi: 10.1016/s0363-5023(03)00148-5.
Results Reference
background
PubMed Identifier
8620634
Citation
Wintman BI, Winters SC, Gelberman RH, Katz JN. Carpal tunnel release. Correlations with preoperative symptomatology. Clin Orthop Relat Res. 1996 May;(326):135-45.
Results Reference
background
PubMed Identifier
17966804
Citation
Ahlberg J, Johansson H, Widenfalk B. [Disabling injuries following carpal tunnel syndrome surgery]. Lakartidningen. 2007 Oct 3-9;104(40):2884-6. No abstract available. Swedish.
Results Reference
background
PubMed Identifier
16952718
Citation
Benson LS, Bare AA, Nagle DJ, Harder VS, Williams CS, Visotsky JL. Complications of endoscopic and open carpal tunnel release. Arthroscopy. 2006 Sep;22(9):919-24, 924.e1-2. doi: 10.1016/j.arthro.2006.05.008.
Results Reference
background
PubMed Identifier
17443508
Citation
Marshall S, Tardif G, Ashworth N. Local corticosteroid injection for carpal tunnel syndrome. Cochrane Database Syst Rev. 2007 Apr 18;(2):CD001554. doi: 10.1002/14651858.CD001554.pub2.
Results Reference
background
PubMed Identifier
34677593
Citation
Hofer M, Ranstam J, Atroshi I. Extended Follow-up of Local Steroid Injection for Carpal Tunnel Syndrome: A Randomized Clinical Trial. JAMA Netw Open. 2021 Oct 1;4(10):e2130753. doi: 10.1001/jamanetworkopen.2021.30753.
Results Reference
derived
PubMed Identifier
24026316
Citation
Atroshi I, Flondell M, Hofer M, Ranstam J. Methylprednisolone injections for the carpal tunnel syndrome: a randomized, placebo-controlled trial. Ann Intern Med. 2013 Sep 3;159(5):309-17. doi: 10.7326/0003-4819-159-5-201309030-00004.
Results Reference
derived
PubMed Identifier
20409331
Citation
Flondell M, Hofer M, Bjork J, Atroshi I. Local steroid injection for moderately severe idiopathic carpal tunnel syndrome: protocol of a randomized double-blind placebo-controlled trial (NCT 00806871). BMC Musculoskelet Disord. 2010 Apr 21;11:76. doi: 10.1186/1471-2474-11-76.
Results Reference
derived

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Steroid Injection Treatment of Carpal Tunnel Syndrome

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