Title

Use of White Granulated Sugar on Wounds
A Randomised Controlled Trial to Investigate the Clinical and Cost-effectiveness of White Granulated Sugar Dressing Compared With Standard Treatment in the Management of Exudating Wounds With Parallel Economic Evaluation
  • Phase

    N/A
  • Study Type

    Interventional
  • Status

    Unknown status
  • Indication/Condition

    Infected Wounds
  • Study Participants

    108
How effective is sugar in reducing the debriding of sloughy, necrotic or infected exudating wounds compared with standard treatment?
Patients for whom all the following apply:

Have an exudating wound sizes 5cm2 and 40cm2 A minimum of 25% slough, infected and necrotic tissue No dry necrotic eschar present Ankle Brachial Pressure Index of greater than 0.6 Are over 18 years Independently and willingly consent
Study Started
Jun 30
2011
Primary Completion
Oct 31
2013
Anticipated
Study Completion
Oct 31
2014
Anticipated
Last Update
Oct 29
2012
Estimate

Other Granulated Sugar

30 grams of granulated sugar is used to cover the wound area and this is held in place using a dry dressing pad , bandage and tape.

  • Other names: Sucrose

Other Debridement Dressing

1 Aquacel or Sorbsan dressing will be put over the wound, and held in place with a dry dressing pad, bandage and tape.

  • Other names: Aquacel or Sorbsan

Chronic & Acute infected wounds Experimental

Wound will be cleaned with normal saline or tap water and Granulated sugar will be applied directly to the wound and covered with an absorbent pad and held in place with a bandage and tape.

Chronic and Acute infected wounds Active Comparator

Wound will be cleaned with normal saline or tap water and an appropriate debridement dressing (Aquacel or Sorbsan) is applied to the wound and secured with a bandage and surgical tape.

Criteria

Inclusion Criteria:

Exudating wound sizes 5cm2 and 40cm2
A minimum of 25% slough, infected and necrotic tissue
No dry necrotic eschar
Ankle Brachial Pressure Index of greater than 0.6
Age over 18 years
Able to independently and willingly consent

Exclusion Criteria:

Participants in a trial evaluating other therapies for their wound
Have previously been in this trial
Women who are pregnant
Participants not able to tolerate daily dressing change
No Results Posted