NCT06124599 Prodromes of Menstrual Staphylococcal Toxic Shock
| NCT ID | NCT06124599 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Hospices Civils de Lyon |
| Condition | Toxic Shock Syndrome Staphylococcal |
| Study Type | OBSERVATIONAL |
| Enrollment | 316 participants |
| Start Date | 2021-12-21 |
| Primary Completion | 2026-12-21 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 316 participants in total. It began in 2021-12-21 with a primary completion date of 2026-12-21.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Menstrual staphylococcal toxic shock is a rare but severe disease, requiring intensive care in over 80% of cases. Menstrual staphylococcal toxic shock develops during the peri-menstrual period, in healthy young women colonized by a vaginal strain of Staphylococcus aureus secreting the Toxic shock syndrome toxin 1 (TSST-1) and not immune to it, in a favorable environment, i.e. wearing intravaginal menstrual protection (tampon, menstrual cup). The rarity of the syndrome, its polymorphous clinical presentation and the absence of a totally specific biological examination make menstrual staphylococcal toxic shock a difficult pathology to diagnose. The reference clinical criteria correspond to the advanced picture of multivisceral failure, making it possible to classify cases a posteriori, but contribute to diagnostic delay and lack sensitivity. Patient accounts suggest the presence of symptoms in the days preceding the development of toxic shock, and also during previous menstrual cycles. The identification of prodromal symptoms could enable earlier management of menstrual staphylococcal toxic shock by removal of intra-vaginal sanitary protection, the main risk factor, before the disease becomes permanently established and requires intensive care.
Eligibility Criteria
Inclusion Criteria : +Case inclusion criteria: * Women between 13 and 30 years old inclusive * Clinical diagnosis of staphylococcal toxic shock syndrome: "confirmed" or "probable" according to Center Disease Control (CDC) criteria: The 5 CDC clinical criteria for menstrual Staphylococcal Toxic Shock are: * a fever above 39°C, * arterial hypotension, * generalized scarlatiniform erythroderma * intense peeling of the palms or soles of the feet 7 to 14 days later, * and systemic manifestations (at least three): * Digestive: vomiting, diarrhea * Muscular: myalgia, increase in serum creatine phosphokinase * Hyperemia of the vaginal, oropharyngeal and conjunctival mucous membranes * Renal: hyperuricemia, hypercreatininemia, leukocyturia without urinary infection, * Hepatic: increase in transaminases * Hematological: thrombocytopenia (\< 100,000 platelets/mm3) * Neurological: apart from episodes of fever or hypotension such as disorientation or altered consciousness. In the presence of 4 criteria, the case is considered probable and 5 criteria as confirmed case. * Detection of S. aureus strain carrying Toxic shock syndrome toxin-1 (TSST1) on vaginal samples. * Onset of symptoms ≤ 72 hours before the start of menstruation and ≥ 72 hours after the end of menstruation. * Use during the last 3 cycles of vaginal protection: tampon or menstrual cup. +Control inclusion criteria: * Women between 13 and 30 years old inclusive * Presence of menstruation * Use of intimate periodic protection, tampon or menstrual cup, during the last 3 periods * No history of toxic menstrual shock Exclusion Criteria: * Non-menstruating women * Women protected by law * Women (or relatives) who oppose the study
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06124599 clinical trial?
This trial is open to female participants only, aged 13 Years or older, up to 30 Years, studying Toxic Shock Syndrome Staphylococcal. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06124599 currently recruiting?
Yes, NCT06124599 is actively recruiting participants. Contact the research team at gerard.lina@chu-lyon.fr for enrollment information.
Where is the NCT06124599 trial being conducted?
This trial is being conducted at Lyon, France.
Who is sponsoring the NCT06124599 clinical trial?
NCT06124599 is sponsored by Hospices Civils de Lyon. The trial plans to enroll 316 participants.