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Study identifier: NCT05428267 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingSEDYC

Sexual Dysfunction in Cirrhosis

Condition: Sexual Dysfunction in Patients With Cirrhosis Awaiting Liver Transplantation  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
WhereParis, France

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The prevalence of erectile dysfunction (ED) is about 10% in the general population, but increases with age, ranging from 9.1% in men 40-49 years to 55% in men \>70. The major risk factors for ED are as follows: diabetes; heart conditions; tobacco use; obesity; injuries to the nerves that control erection; medications such as antidepressants; psychological conditions such as stress, anxiety, or depression; and drug or alcohol use (4). The International Index of Erectile Function (IIEF5) is a simple and well-validated tool for the evaluation of ED (5) and is considered the gold standard for the diagnosis and evaluation of symptom severity. The link between cirrhosis and ED has been suggested in a recent study, showing ED was also impacted by liver failure, portal hypertension and other known risk factors. In the investigators team, they showed, additionally, that neurocognitive impairment is associated with ED in cirrhosis (data not published). The prevalence of ED after liver transplantation (LT) varies among series, ranging from 66 to 86%. After LT, on the one hand, improvement of liver function and bioavailable testosterone favours the improvement of ED. On the other hand, immunosuppressive agents are suspected to worsen it. ED's reversibility has also been discussed; nevertheless, data are scarce and heterogeneous. In the investigators group, they can perform in routine a neurocognitive evaluation of patients with cirrhosis thanks to a neuropsychologist experienced in co…

This description comes directly from the study's public registry record.

Talk to the study team

Marika Rudler, MD, PhD  ·  +33142161454  ·  marika.rudler@aphp.fr

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * (1) cirrhosis; (2) non-urgent indication for LT. Exclusion Criteria: * (1) clinical HE; (2) dementia; (3) language barrier; (4) past history of prostatic surgery

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Service d'hépato-gastroentérologie Hôpital Pitié-SalpêtrièreParis, FranceRecruiting

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