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The Role of Skin Microbiota in Hepatic or Renal Pruritus

Recruiting
Conditions
Renal Failure
Hepatic Failure
Pruritus
Interventions
Diagnostic Test: Isolation of skin microbiota
Registration Number
NCT05604469
Lead Sponsor
Zagazig University
Brief Summary

* Various neurotransmitters may share in the pathogenesis of hepatic and renal itching.

* Skin microbiota may share in the pathogenesis of pruritus.

Detailed Description

Uremic pruritus (UP) is a frequent phenomenon and it is regarded as one of the most bothersome symptoms in patients with chronic renal disease. The prevalence of UP is still high and reported in around 40% to 50%. UP has an important impact on patients' quality of life and sleep, depression, and increased mortality. The pathogenesis of UP remains blurry, although many different factors have been indicated in the etiology of this symptom, including increased systemic inflammation, abnormal serum parathyroid hormone, calcium, and phosphorus levels, an imbalance in opiate receptors, a neuropathic process, or even skin dryness. This is why until now there is no specific treatment for patients with UP and many of the available therapeutic modalities are not satisfactory Pruritus in liver diseases can often be a debilitating symptom causing significant impairment in quality of life. Not all patients with liver disease develop pruritus and its prevalence varies depending on the underlying cause of liver disease. It is more common in conditions characterized by bile duct inflammatory destruction than in those characterized by hepatocellular injury.

Cutaneous microbiota delivers a diverse and far-reaching influence on our physiology by calling upon the host nervous system. Bacteria make metabolites, toxins, and structural components that are recognized by peripheral and central neurons via matching receptors. Microbiota also indirectly affects neural function by causing endocrine (i.e., keratinocytes) and immune cells to transmit signals (i.e., cytokines, proteases). Itch is a prototypic sensory neural function, and the microbiota propels the itch-scratch cycle.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Patients of both sexes. Patients with hepatic illness (autoimmune liver diseases, chronic viral hepatitis, and drug-induced liver injury) or Patients with renal failure Willing to sign an informed consent.
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Group A (liver faluire patients with pruritus)Isolation of skin microbiotaPatients with hepatic illness (autoimmune liver diseases, chronic viral hepatitis, and drug-induced liver injury)
Group D (renal faluire patients without pruritus)Isolation of skin microbiota-
Group C (renal faluire patients with pruritus)Isolation of skin microbiota-
Group B (liver faluire patients without pruritus)Isolation of skin microbiotaPatients with hepatic illness (autoimmune liver diseases, chronic viral hepatitis, and drug-induced liver injury)
Primary Outcome Measures
NameTimeMethod
To evaluate the possible change of skin microbiota in patients with renal or hepatic pruritus8 weeks

Isolation of skin microbiota including, Staphylococcus epidermidis, Propionibacterium acnes, Pseudomonas aeruginosa, Staphylococcus aureus, Streptococcus pyogenes and Candida.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Reham Essam

🇪🇬

Zagazig, Al Sharqia, Egypt

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