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Behandeling van jeukklachten bij brandwondpatiënten met doxepine crème

Standard Topical Ointment or doxepin against Pruritus in burn patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25977
Enrollment
27
Registered
2017-03-03
Start date
2017-05-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Itch, burns, jeuk, brandwonden

Interventions

Patients will be randomized to start with either the doxepin cream or the placebo cream. Patients will be required to use the cream at least once daily for two consecutive weeks. This is followed by a

Sponsors

Prof. E. Middelkoop, PhD Association of Dutch Burn Centres Zeestraat 27-29, 1941 AJ Beverwijk
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Age ≥ 18 years - Healed burns - Itch with an intensity ≥ 3 as determined by the VAS score for itch at time of the enrolment - Treatment in one of the three Dutch burn centres - Total area that itches must not exceed >10% TBSA

Exclusion criteria

Exclusion criteria: - Unable to give informed consent - Unable to understand and fill in VAS scores and questionnaires (as determined by the treating burn physician) - Cutaneous or systemic disease causing itch - Any diseases or condition that is associated with adverse effects using doxepin, that is: Hypersensitivity to any of its components, Glaucoma, A tendency to urinary retention, Sever liver disease, Mania, Sever heart disease (including cardiac arrhythmias), Pregnancy and lactation

Design outcomes

Primary

MeasureTime frame
The main study parameter is the change in pruritus intensity as measured by the Visual Analogue Scale (VAS), with a decrease of ≥2 point being defined as clinically significant.

Secondary

MeasureTime frame
The secondary study parameters include the determination of the MIC of the itch scores, the characteristics and impact of itch as measured by the BIQ, and scar quality as measured by the POSAS. Other study parameters include: the use of hydrating cream, use of escape medication and use of pressure garments. Furthermore, we will register sex, age, medical history, cause of burn, location of burn wound, %TBSA burned, time to wound healing (will be estimated retrospectively), % burn wound area that itches, duration of itch, itch before inclusion and wound treatment (conservative or surgery).

Contacts

Public ContactKelly Kwa
kkwa@rkz.nl0251-265741

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)