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Cryotherapy versus Salicylic Acid with Monochloracetic Acid for the Treatment of Verrucae: A Randomised Controlled Trial
ISRCTN ISRCTN78267267
ClinicalTrials.gov identifier
Public title Cryotherapy versus Salicylic Acid with Monochloracetic Acid for the Treatment of Verrucae: A Randomised Controlled Trial
Scientific title
Acronym N/A
Serial number at source N0530132857
Study hypothesis Verrucae, or warts, are a common, infectious and sometimes painful problem, but it is uncertain which is the most effective treatment. We plan to compare two commonly used treatments for warts: salicylic acid with monochloracetic acid or cryotherapy. We are interested to know how effective the two treatments are in cleaning up the warts and also how cost effective the two treatments are compared to one another. Patients will also be asked about acceptability with their treatment and possible side effects such as pain.
Lay summary Not provided at time of registration
Ethics approval Not provided at time of registration
Study design Randomised controlled trial
Countries of recruitment United Kingdom
Disease/condition/study domain Skin and Connective Tissue Diseases: Warts
Participants - inclusion criteria Not provided at time of registration
Participants - exclusion criteria Not provided at time of registration
Anticipated start date 29/10/2003
Anticipated end date 31/08/2004
Status of trial Stopped
Patient information material
Target number of participants 133 in each treatment group
Interventions Database analysis, Questionnaires, Randomised Controlled Trial - to compare:
1. Cryotherapy
2. Salicylic acid with monochloracetic acid
For treatment of plantar warts

August 2008: Trial stopped 2006.
Primary outcome measure(s) A recent systematic review has highlighted the uncertainty with respect to the optimal treatment of verrucae and warts (Gibbs Set et al, BMJ, 2002). Freezing warts using cryotherapy is widespread but there is little evidence showing it is effective. However, it may be relatively cost effective compared with chemical treatments in that fewer visits may be required to eradicate the condition. There is a need for a randomised controlled trial with a cost effectiveness analysis to ascertain which is the best approach. The evidence base would aid clinical decision makers and also health care managers in resource allocation
Secondary outcome measure(s) Not provided at time of registration
Sources of funding North Central London Research Consortium (UK)
Trial website
Publications
Contact name Miss  Julie C  Day
  Address Podiatry Department
First Floor East Wing
St Pancras Hospital
4 St Pancras Way
  City/town London
  Zip/Postcode NW1 0PE
  Country United Kingdom
  Tel +44 (0)20 7530 3871
  Email jules.day@virgin.net
Sponsor Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
  Address The Department of Health,
Richmond House,
79 Whitehall
  City/town London
  Zip/Postcode SW1A 2NL
  Country United Kingdom
  Tel +44 (0)20 7307 2622
  Email dhmail@doh.gsi.org.uk
  Sponsor website: http://www.dh.gov.uk/Home/fs/en
Date applied 30/09/2004
Last edited 27/09/2011
Date ISRCTN assigned 30/09/2004
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