Probiotics and Activated Charcoal for Uremic Pruritus in Chronic Kidney Disease
Probiotic Blend Capsule
+ Activated Charcoal
Urogenital Diseases+15
+ Anthrax
+ Bacterial Infections and Mycoses
Treatment Study
Summary
Study start date: September 1, 2024
Actual date on which the first participant was enrolled.Chronic kidney disease-associated pruritus is an uncomfortable condition that leads to a persistent need to scratch, significantly affecting the quality of life for those with chronic kidney disease. This study aims to explore whether probiotics or activated charcoal can help manage this skin itching problem. By investigating ways to reduce the levels of certain toxins in the body that contribute to this itchiness, this study hopes to find more effective treatments. Probiotics might help by improving the balance of good bacteria in the body, while activated charcoal may work by absorbing these toxins before they get into the bloodstream. Participants in this study will receive either probiotics or activated charcoal. Probiotics are taken orally and work by enhancing the gut's bacterial environment, potentially leading to improvements in skin conditions. Activated charcoal, also taken orally, acts by capturing toxins within the digestive system, thus reducing their levels in the blood. The effectiveness of these treatments will be evaluated based on how much they can reduce the sensation of itching and improve the participants' overall quality of life. Both treatments are being tested for their ability to offer relief without causing serious side effects.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.123 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 75 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives