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Transgender, Silicone and Blood Smear

Circulating Silicone After Cosmetic Silicone Injection in Transgender Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02580760
Acronym
TSBS
Enrollment
66
Registered
2015-10-20
Start date
2015-07-31
Completion date
2016-01-31
Last updated
2016-01-25

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

Conditions

Injection; Complications, Sepsis, Injection Site Disorder, Injection Site Extravasation, Intentional Poisoning by Silicone

Keywords

Silicone, Transgender, Dermatology, Blood contamination, Adverse event after injection

Brief summary

This cross-sectional monocentric study will describe transgender men transitioning into women and who had cosmetic silicone injection. The principal objective is to estimate the prevalence of Transgender with circulating monocytes containing silicone vacuoles in blood smears among Male to Female Transgender population with a history of cosmetic silicon injections. The secondary objectives are to describe the transgender population, to describe the quantity of silicone in vacuoles of circulating monocytes, and the association between dermatological complications (inflammatory and not inflammatory) and several clinical and biological characteristics (HIV status, level of immunosuppression, inflammatory syndrome, quantity of silicone which was injected , silicone quantity in blood smears).

Detailed description

Injectable liquid silicone is a permanent filling product which is no more used in France because of a high risk of complications. Cosmetic silicone injection is a common feminization approach for transgender populations. This cross-sectional monocentric study will describe transgender men transitioning into women and who had cosmetic silicone injection. The principal objective is to estimate the prevalence of Transgender with circulating monocytes containing silicone vacuoles in blood smears among Male to Female Transgender population with a history of cosmetic silicon injections. The secondary objectives are to describe the transgender population, to describe the quantity of silicone in vacuoles of circulating monocytes, and the association between dermatological complications (inflammatory and not inflammatory) and several clinical and biological characteristics (HIV status, level of immunosuppression, inflammatory syndrome, quantity of silicone which was injected , silicone quantity in blood smears).

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults * Not in opposition to data collection * Transgender men transitioning into women patients with cosmetic silicone injection * Consultation in Bichat hospital

Exclusion criteria

* Unable to communicate * Guardianship, curatorship

Design outcomes

Primary

MeasureTime frameDescription
The prevalence of Transgender with circulating monocytes containing silicone vacuoles in blood smear among Male to Female Transgender population, the day of their consultation.1 day ,the day of their consultationThe prevalence of Transgender with circulating monocytes containing silicone vacuoles will be calculated as the number of subjects with monocytes containing silicone vacuoles in blood smears on the number of subjects with a history of silicone cosmetic injection

Secondary

MeasureTime frameDescription
Size of silicone vacuoles in monocytes1 day ,the day of their consultation
Inflammatory and not inflammatory dermatological complications1 day ,the day of their consultationassessment of dermatological complications during the clinical examination
Number of patients with a positive HIV status1 day ,the day of their consultationNumber of patients with a positive HIV status
Level of immunosuppression estimated with viral charge1 day ,the day of their consultationHIV viral load, the day of the admission or the last value known in the 6 month prior to the consultation
Level of immunosuppression estimated with cluster of differentiation 4 cell (CD4) rate1 day ,the day of their consultationCD4 cell count the day of the consultation or the last value known in the 6 month prior to the consultation. CD4 cell stands for Cluster of differentiation antigen 4 cell.
Inflammatory syndrome estimated with C-reactive protein (CRP)1 day ,the day of their consultation
Number of monocytes with vacuoles of silicone in a standardized area of 25 monocytes per blood smear slide1 day ,the day of their consultation
Amount of injected silicone, in liters1 day ,the day of their consultation
Time since the first silicone injection for cosmetic purposes, in years1 day ,the day of their consultation
Comorbidities: Number of patients with history of Tuberculosis1 day ,the day of their consultationNumber of patients with history of Tuberculosis
Comorbidities: Number of patients with history of Hepatitis B1 day ,the day of their consultationNumber of patients with history of Hepatitis B
Comorbidities: Number of patients with history of Hepatitis C1 day ,the day of their consultationNumber of patients with history of Hepatitis C
Comorbidities: Number of patients with history of Syphilis1 day ,the day of their consultationNumber of patients with history of Syphilis
Inflammatory syndrome estimated with ferritin1 day ,the day of their consultation

Countries

France

Outcome results

None listed

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