Desensitisation: does it reduce scar sensitivity following carpal tunnel release?

ISRCTN ISRCTN97616350
DOI https://doi.org/10.1186/ISRCTN97616350
Protocol serial number N0264120265
Sponsor Department of Health (UK)
Funder United Bristol Healthcare NHS Trust (UK)
Submission date
12/09/2003
Registration date
12/09/2003
Last edited
28/04/2015
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Nervous System Diseases
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Ms Fiona Powell
Scientific

c/o Research and Development Office
Level 1, Old Building
Bristol Royal Infirmary
Marlborough Street
Bristol
BS2 8HW
United Kingdom

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Scientific titleDesensitisation: does it reduce scar sensitivity following carpal tunnel release?
Study objectivesTo investigate whether a short, therapy-led desensitisation programme reduces scar sensitivity following carpal tunnel release.
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedNervous System Diseases: Carpal tunnel syndrome (CTS)
Intervention1. Evaluation plus standard care
2. Evaluation, standard care plus a desensitisation programme and advice sheet
Intervention typeOther
Primary outcome measure(s)

Not provided at time of registration

Key secondary outcome measure(s)

Not provided at time of registration

Completion date01/09/2003

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit18 Years
SexAll
Target sample size at registration24
Key inclusion criteria24 patients aged 18 to 85 with a history of uncomplicated, idiopathic carpal tunnel syndrome will be included in this study.
Key exclusion criteriaNot provided at time of registration
Date of first enrolment01/10/2002
Date of final enrolment01/09/2003

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Bristol Royal Infirmary
Bristol
BS2 8HW
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan