Actively Recruiting
LOng COvid COmorbidities: Andrological, Reproductive, Sexual Dysfunctions in Patients Recovered From COVID-19
Led by Federico II University · Updated on 2025-08-11
100
Participants Needed
1
Research Sites
260 weeks
Total Duration
On this page
Sponsors
F
Federico II University
Lead Sponsor
A
Azienda Sanitaria Locale Napoli 2 Nord
Collaborating Sponsor
AI-Summary
What this Trial Is About
Considering the compelling amount of studies focused on patients in the active phase of COVID-19 disease and the scarcity of studies focused on patient cured from disease aimed at evaluating the sequelae of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection, the purpose of the study is to investigate, in patients recovered from COVID-19 disease: 1) whether SARS-CoV-2 infection has induced in male patients, a primary (testicular) and / or secondary (pituitary) damage to the hypothalamic-pituitary-testicular hormonal axis, structural and / or functional damage to the testis and penis, sexual dysfunction or fertility disorders; 2) the prevalence in male and female patients of chemosensory symptoms (olfactory dysfunction) and assess whether there is a correlation between the prevalence, severity, duration and eventual persistence of olfactory dysfunction and the severity of COVID-19 disease. Patients will be evaluated at baseline (at discharge from infectious and/or pneumology unit) and after 3- 12 months. A better definition of the prevalence and type of sequelae after recovery from COVID-19 disease could significantly improve the therapeutic management and long-term follow-up of these patients, with a relevant impact in terms of health resources and public health.
CONDITIONS
Official Title
LOng COvid COmorbidities: Andrological, Reproductive, Sexual Dysfunctions in Patients Recovered From COVID-19
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients of both sexes recovered from SARS-CoV-2 infection (two negative nasopharyngeal swabs, negative IgM and positive anti SARS-CoV-2 IgG)
- Aged over 18 years of age
- Ability to understand protocol procedures
You will not qualify if you...
- Any psychological, psychiatric, or other medical conditions that impair understanding of the study's nature, purpose, or consequences
- Uncooperative attitude of the patient
AI-Screening
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Trial Site Locations
Total: 1 location
1
Federico II University of Naples
Naples, Italy, Italy, 80131
Actively Recruiting
Research Team
R
Rosario Pivonello, Prof.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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