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Transillumination to Reduce Post-injection Complications in Aesthetic Medicine

Transillumination: A Non Invasive Method to Reduce Complications Associated With Facial Injections in Aesthetic Medicine.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04750421
Enrollment
72
Registered
2021-02-11
Start date
2018-03-01
Completion date
2018-07-01
Last updated
2021-02-15

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

Conditions

E05.642.500

Keywords

transillumination, Aesthetic injection, asthetic post-injection complications, hyaluronic acid, Facial injection

Brief summary

Transillumination (TL) is a noninvasive technique that appears to allow preliminary detection of superficial vascular structures of the face to avoid intravascular HA injection. The purpose of our study was to test the efficacy of TL in terms of its sensitivity to locate vessels in the areas undergoing treatment and to reduce post-injection vascular complications.

Detailed description

Transillumination was used during the injection of hyaluronic acid to reduce the risk of intravascular injection. For the purpose of randomization, patients were asked to choose a sealed envelope. Inside the envelope was a piece of paper indicating on which side of the face (right or left) the transillumination would be used. For each filler injection, transillumination was used on one side; on the other side of the face, the injection was administered without the use of any vascular exploration method. After the vessels had been located on the side chosen for the transillumination technique, a skin-marker pencil was used to draw the vascular mapping of the upper part of the face, which in our opinion represented the area most at risk of complications, the middle and the lower parts of the face. Then ice was applied on both sides of the face for 15 s before to proceed with the injections in order to cause vasoconstriction and to further decrease the risk of an intravascular injection.Transillumination sensitivity for locating the vessels of the face was assessed.

Interventions

DEVICETransillumination Venolux®

Transillumination Venolux® method was used on the other half of the face before injections to visualize veins.

Sponsors

Helynck, Patrick, M.D.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

The operator will guarantee the confidentiality of the part of facial where the trasillumination was used, the assessors will not be aware of the part of the face where the transillumination was used.

Intervention model description

The random assignment of the right or left side of the face on which the trasnillumination will be used will be done by numbered and sealed envelope. Envelopes will be prepared before the start of inclusion. Each envelope will contain a sheet of paper whose contents cannot be guessed when the envelope is closed. Each sheet will be marked either Left+TL or Right+TL. Each envelope will contain a unique code number that will be randomly assigned to each patient after inclusion.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients presenting for facial injections of hyaluronic acid

Exclusion criteria

* Patients with a history of allergy to a component of hyaluronic acid * Patients with arteritis (Horton) * Patients who have had previous facial surgery * pregnant or nursing patients

Design outcomes

Primary

MeasureTime frameDescription
Number of vessels detected by using transilluminationBefore facial injectionscounting the number of vessels detected by using transillumination in relation to the number of existing vessels.

Secondary

MeasureTime frameDescription
Number of bruises and hematomaAt day 3 after facial injectionsNumber of bruises and heamatoma post-injection in in the hemiface where Transillumination is used versus control hemiface

Countries

France

Outcome results

None listed

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