NCT06745245Active, not recruiting
Effect of Oral Consumption of a Symbiotic Gelatin on the Presence of Gastrointestinal Symptoms and Quality of Life in People With Chronic Kidney Disease
Effect of Oral Consumption of a Symbiotic Gelatin on the Presence of Gastrointestinal Symptoms and Quality of Life in People With Chronic Kidney Disease Grades G3a, G3b, G4, G5 and G5D in Mexico
Source: ClinicalTrials.gov · Last updated 20 Dec 2024
Brief summary (registry, in English)
In patients with chronic kidney disease (CKD) there is a high prevalence of gastrointestinal disorders and negative changes in the microbiota and assimilation of nutrients, which is associated with an increased risk of morbidity and mortality.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 32 (estimated)
- First submitted
- 18 Oct 2024
- Start date
- 12 Sept 2024
- Primary completion date
- 12 Sept 2025
- Lead sponsor
- NIN Institute
- Diseases
- Chronic kidney disease
- NCT number
- NCT06745245
What you commit to
- Study type: Interventional
- Planned participants: 32
- From 12 Sept 2024 to the primary completion date, 12 Sept 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Failure to attend evaluation and biochemical tests at the beginning and end of the study.
Other
- Non-compliance with ≥ 10% of probiotics + fiber intakes (≥ 3 sachets in 15 days) during the intervention period.
- Identification of serious adverse effects.
- Withdrawal of voluntary participation by the patient.
Who the study is looking for
- Previous hospitalizations in the last month.
- Diagnosis of comorbidities such as cancer, decompensated heart failure, decompensated lung disease, decompensated liver disease, HIV, infection present within the last 3 months (chronic and/or acute) stroke, malabsorption syndrome or allergy to any ingredient of the nutritional supplement.
- Colon surgeries in the past 6 months (obstruction, resection of a portion).
- Presence of ostomies.
- Who show current treatment of antibiotics or oral iron.
Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Centro Médico Issemym Coordinator of this site? Confirm its status | Toluca | Mexico | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.