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Less Frequency Hemodialysis and COVID-19

Reduced Frequency Hemodialysis in Prevalent Patients Due to the Coronavirus Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04374058
Enrollment
50
Registered
2020-05-05
Start date
2020-03-20
Completion date
2021-03-31
Last updated
2020-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End Stage Renal Disease

Keywords

Covid-19, Dialysis, less frequency hemodialysis, Ultrafiltration rate, Anemia, Nutrition

Brief summary

Facing the unusual situation imposed by the coronavirus disease, the aim of this study is to evaluate the risk and effects of less frequent hemodialysis on prevalent patients

Detailed description

The novel coronavirus disease (COVID-19), also known as COVID-19 (and SARS-Cov2) by the World Health Organization, is a rapidly evolving pandemic. The outbreak is expected to infect a large portion of the world population, and a case fatality rate of 1-3% represents a significant mortality and healthcare burden. In common with other viral diseases, mortality is higher in elderly patients with high comorbidity. The impressive figures of transmission in different communities underline the need for reorganization of efforts to limit contagion, particularly in crowded settings. Hemodialysis centres represents a specific setting in which many patients are repeatedly treated in the same area at the same time. Dialysis patients constitute a susceptible population because of their older age, high comorbidity burden and their less efficient immune system. Therefore, they are more prone to develop severe infectious diseases than the general population.. Moreover, if infected, the requirements of specialized resources and staff is further complicated by requirements for isolation, control and prevention, putting healthcare systems under additional strain. Therefore, all measures to slow and to control unmanageably high incidence rates must be taken very seriously. The routine treatment usually requires three dialysis sessions per week Further, some patients must travel long distances to the dialysis centre. One option to reduce the higher risk of these patients is to reduce the frequency of dialysis sessions.However, the potential benefits of reduced risk may be associated with higher interdialytic weight gain and inadequate dialysis, Two factors that increase the risk of mortality. Furthermore, the impact of reduced frequency on Anemia and Nutrition have not been extensively studied.

Interventions

OTHERless-frequency hemodialysis

Patients of treatment group would be evaluated quarterly

Sponsors

Dialisis Madariaga
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* More than 30 days of Chronic ambulatory in-center hemodialysis

Exclusion criteria

* More than three sessions a week * amputated lower limbs

Design outcomes

Primary

MeasureTime frameDescription
MortalityFrom date of beginning of the study until the date of death assessed up to 52 weeksTime to all-cause and cardiovascular death

Secondary

MeasureTime frameDescription
Anemia, Nutrition, Adequation of dialysis, total ultrafiltration, ultrafiltration rate,From date of beginning of the study assessed up to 52 weeksTime variation of the biological parameters mentioned in the title. Repeated measurements of laboratory variables will be averaged into patient quarterly means to minimize measurement variability.
HospitalizationFrom date of beginning of the study until the date of first hospitalization assessed up to 52 weeksTime to first hospitalization of any cause
Vascular AccessFrom date of beginning of the study until the date of first intervention assessed up to 52 weeksTime to first endovascular or quirurgical intervention of the vascular access utilized at the start of the study

Countries

Argentina

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026