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. 2017 Jul 12;2017(7):CD011821. doi: 10.1002/14651858.CD011821.pub2

Phipps 1988.

Methods Country where data collected: UK
Parallel group RCT
Unit of randomisation: participant
Unit of analysis: participant
Duration: NR
Participants Inclusion criteria: burns less than 5% TBSA (averaging under 1%) suitable for outpatient treatment
Exclusion criteria: those needing inpatient treatment, facial burns, hand burns managed in bags and those whose treatment was to be continued elsewhere
Participants: 196 outpatients
Mean age (years): < 5 years: 21 vs 24; 5‐14 years: 7 vs 9; > 14 years: 64 vs 71
Male participants: 49 vs 64
Burn type: NR
Burn degree: NR
Burn size (%TBSA): < 1%
Burn location: NR
Interventions Intervention arm 1: hydrocolloid material covered with cotton gauze overlaid with cotton wool and secured with crepe bandage or adhesive tape. Dressing inspected on 3rd or 4th day and then changed weekly unless dressing contaminated or adverse symptoms developed
Intervention arm 2: chlorhexidine‐impregnated tulle‐gras dressing covered with cotton gauze overlaid with cotton wool and secured with crepe bandage or adhesive tape. Dressing inspected on 3rd or 4th day and then changed weekly unless dressing contaminated or adverse symptoms developed
Cointerventions: NR
Outcomes Primary outcome: wound healing
Primary outcome: infection
Notes Funding NR
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Quote: “patients were allocated randomly to one of two treatment groups”
Comment: no further information on method of randomisation
Allocation concealment (selection bias) Unclear risk Quote: “patients were allocated randomly to one of two treatment groups”
Comment: no further information to indicate concealment of allocation
Blinding of outcome assessment (detection bias) 
 All outcomes Unclear risk Quote "at each inspection of the wound, its progress towards healing was noted"
Comment: no indication that outcome assessment was blinded but unclear
Incomplete outcome data (attrition bias) 
 All outcomes High risk Quote: “119 of the 196 patients were followed to complete healing”
Comment: details were given on why the excluded participants' data were not included
Selective reporting (reporting bias) Low risk Comment: no direct quotes but all stated outcomes of interest were reported
Other bias Unclear risk Comment: no direct quotes but no evidence of additional sources of bias but reporting insufficient to be certain