Evidence map›Paper›PMID 31455398›Full record

ArticleTrials2019

Treatment of carpal tunnel syndrome with wrist splinting: study protocol for a randomized placebo-controlled trial.

Isam Atroshi, Kamelia Tadjerbashi, Steven J McCabe, Jonas Ranstam

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Splinting for carpal tunnel syndrome.The Cochrane database of systematic reviews · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Isam AtroshiDepartment of Clinical Sciences - Orthopedics, Lund University, SE-22100, Lund, Sweden. isam.atroshi@med.lu.se.ORCID http://orcid.org/0000-0003-4892-9890
Kamelia TadjerbashiDepartment of Clinical Sciences - Orthopedics, Lund University, SE-22100, Lund, Sweden.
Steven J McCabeDepartment of Surgery, University of Toronto, Toronto Western Hospital, Toronto, ON, M5T 2S8, Canada.
Jonas RanstamDepartment of Clinical Sciences - Orthopedics, Lund University, SE-22100, Lund, Sweden.
Lund University · SEUniversity of Toronto · CA

Funding

Governmental Funding of Clinical Research within the National Health Service (ALF) 2018-0251
6 · The paper itself

Abstract

backgroundCarpal tunnel syndrome (CTS) is a common cause of pain, weakness, sensory loss, and activity limitations. Currently, the most common initial treatment is use of a rigid splint immobilizing the wrist, usually during night-time, for several weeks. Evidence regarding the efficacy and effect durability of wrist splinting is weak. The treatment is associated with costs and may cause discomfort and limit daily and work activities. No placebo-controlled trials have been performed.

methodsThis is a randomized controlled trial designed to assess the efficacy of a rigid wrist splint compared with soft wrist bandage (placebo) in patients with primary idiopathic CTS. The trial will be conducted at an orthopedic department. Patients, 25 to 65 years old, who seek primary health-care with symptoms of CTS will be screened, and potentially eligible patients will be referred to the study center. Patients who fulfill the trial's eligibility criteria will be invited to participate. A total of 112 patients who provide informed consent will be randomly assigned to treatment with either a rigid wrist splint or a soft bandage to be used initially for 6 weeks at night and, if possible, during the day. The splints and bandages will be fitted with a temperature-monitoring device to measure the total time during which they have actually been worn. The trial participants will complete a questionnaire that includes the 6-item CTS symptoms scale (CTS-6); the 11-item disabilities of the arm, shoulder, and hand (QuickDASH) scale; and the EuroQol 5-dimension (EQ-5D) health status and quality-of-life measure at baseline and at 6, 12, 24, and 52 weeks after treatment start. The participants will undergo physical examination and nerve conduction testing at baseline and at 52 weeks. The trial's primary outcomes are the change in the CTS-6 score from baseline to 12 weeks and the rate of carpal tunnel release surgery at 52 weeks. DISCUSSION: This is the first placebo-controlled randomized trial with electronic monitoring of actual splint use and will provide evidence regarding the efficacy of wrist splinting in patients with CTS.

trial registrationISRCTN Registry, ISRCTN81836603 . Registered on May 5, 2018.

Indexed as

SplintsAdultAgedCarpal Tunnel SyndromeDisability EvaluationEquipment DesignFemaleHumansMaleMiddle AgedOrthopedic ProceduresProspective StudiesQuality of LifeRandomized Controlled Trials as TopicRecovery of FunctionSwedenCarpal tunnel syndromeCTSMedian nerveNon-surgical treatmentRandomized trialRCTSplintingWrist

Identifiers

PMID31455398
PMCPMC6712840
OpenAlexW2970250708

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.