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NCT02761174

Topical Brimonidine to Reduce Inflammation After IPL-treatment in Patients With Facial Telangiectasias

Completed Phase 4 Last updated 5 January 2018
What this trial tests

Phase 4 trial testing Brimonidine in Telangiectasias in 19 participants. Completed in 13 January 2017.

Timeline
13 March 2016
Primary endpoint
11 July 2016
13 January 2017

Quick facts

Lead sponsorMerete Haedersdal
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment19
Start date13 March 2016
Primary completion11 July 2016
Estimated completion13 January 2017
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

Merete Haedersdal — full company profile →

Who can join

Adults 18 to 65, any sex, with Telangiectasias. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to investigate whether brimonidine cream can reduce IPL-induced inflammation in terms of redness, swelling and pain in patients with facial vascular lesions (telangiectasias). Furthermore, the effect of brimonidine cream on IPL-efficacy is evaluated one month after final IPL-treatment. The hypothesis is that brimonidine, which has been proved effective in reduction of symptomatic erythema in patients with rosacea, also may have the ability to reduce IPL-induced erythema. Since the potential reduction in erythema is caused by vasoconstriction, brimonidine may further reduce IPL-induced oedema and pain.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Role of adrenergic receptor signalling in neuroimmune communication.
    Chhatar S, Lal G. · · 2021 · cited 76× · PMID 35492402 · DOI 10.1016/j.crimmu.2021.11.001

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Other trials of Brimonidine

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