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Water for Reducing Pain in Negative Pressure Wound Therapy

Cold Water for Reducing Pain in Negative Pressure Wound Therapy Dressing Change

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02820272
Enrollment
27
Registered
2016-06-30
Start date
2012-10-31
Completion date
2013-09-30
Last updated
2016-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Treatment

Keywords

Cold water, Negative pressure wound therapy, pain

Brief summary

Negative pressure wound therapy (NPWT) is a technique using vacuum dressing to promote wound healing in complicated wound. However for many patients, the application and removal of the NPWT is source of procedural pain. Some techniques had been reported to reduce these pain such as administering topical lidocain or normal saline solution before the dressing change. The authors hypothesized that administering cold water into the NPWT sponge would decrease pain during dressing changes.

Interventions

PROCEDURENPWT with cold water

Each of dressing change would be treated with NPWT and injection of cold sterile water kept in 4°C temperature into sponge 10 minutes before dressing change

PROCEDURENPWT with normal saline room temp

Each of dressing change would be treated with NPWT and injection of room temperature sterile water kept in room temperature into sponge 10 minutes before dressing change

PROCEDURENPWT without other intervention

Each of dressing change would be treated with NPWT without injection of any liquids into sponge before dressing change

Sponsors

Chulalongkorn University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Open wounded patient who is treated by negative pressure wound therapy (NPWT) with the age between 18-70 years old.

Exclusion criteria

* The patient who has decrease sensation at cured wound region * The patient who has Glasgow coma scale less than 15 * The patient who cannot provide pain scale data * The patient who has diabetic ulcer or other chronic sores * The patient who denies to participate in research project.

Design outcomes

Primary

MeasureTime frame
Pain reduction during dressing changes assessed by Visual Analogue Scale (VAS)3 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026