A double-blind randomised controlled trial of the efficacy of low level laser therapy on wound healing following nail surgery

ISRCTN ISRCTN63833651
DOI https://doi.org/10.1186/ISRCTN63833651
Protocol serial number RDC01733
Sponsor NHS R&D Regional Programme Register - Department of Health (UK)
Funder NHS Executive London (UK)
Submission date
23/01/2004
Registration date
23/01/2004
Last edited
16/06/2014
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Skin and Connective Tissue 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

Mrs Alysia Kirby
Scientific

Diabetic Centre
Whipps Cross Hospital
Whipps Cross Road
London
E11 1NR
United Kingdom

Phone +44 (0)20 8970 8241

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Study type Participant information sheet
Scientific title
Study objectives1. To compare the efficacy of low level laser therapy with conventional wound dressing on wound healing following nail surgery
2. To show whether low level laser therapy reduces pain levels compared to conventional wound dressing
3. To evaluate the cost effectiveness of low level laser therapy in terms of drug and dressing uptake and return appointments
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedSkin and connective tissue diseases
Intervention1. Low level laser therapy
2. Conventional wound dressing
Intervention typeOther
Primary outcome measure(s)

1. Assessments of wound size
2. Level of inflammation
3. Level of exudate

Key secondary outcome measure(s)

Not provided at time of registration

Completion date01/04/2003

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexNot Specified
Key inclusion criteriaPatients referred to the chiropody clinic, who are going to have one or more toenails removed and who have given informed consent will be randomised into one of two treatment groups
Key exclusion criteriaNot provided at time of registration
Date of first enrolment01/10/2001
Date of final enrolment01/04/2003

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Diabetic Centre
London
E11 1NR
United Kingdom

Results and Publications

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

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Participant information sheet Participant information sheet 11/11/2025 11/11/2025 No Yes