Survival on Peritoneal Dialysis (PD) Versus Hemodialysis (HD) in China

Baxter

Status and phase

Terminated

Phase 4

Conditions

End Stage Renal Disease

Treatments

Other: Peritoneal Dialysis treatment

Other: Hemodialysis treatment

Study type

Interventional

Funder types

Industry

Identifiers

NCT01413074

CHN-RENAL-CTPIV-2010-106

Details and patient eligibility

About

Primary Objective: The primary objective is to prospectively assess and compare survival in subjects with End Stage Renal Disease (ESRD) randomized to Peritoneal Dialysis (PD) or Hemodialysis (HD) treatment.

Secondary Objectives: The secondary objectives are to prospectively assess and compare the following parameters in subjects receiving PD or HD treatment:

Technique failure
Cause of death
Comorbidity status at baseline and changes throughout the study
Change in residual renal function (RRF)
Dialysis adequacy (i.e., Kt/Vurea)
Change in blood pressure, hemoglobin, and S-phosphate
Change in nutritional status
Occurrence of bacterial and other infections
Hospitalization, including number, duration, and underlying reason(s)
Systemic inflammation as assessed by high-sensitivity C reactive protein (hs-CRP)
Quality of life (QOL)

Safety Objectives: To compare the nature and frequency of adverse events (AEs) and serious adverse events (SAEs), including abnormal laboratory test findings with clinical significance, in subjects receiving PD or HD treatment.

Enrollment

416 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects of either sex, aged 18 years or older at time of randomization.
Subjects diagnosed with ESRD (glomerular filtration rate [GFR] ≤ 15 mL/min/m2 body surface area [BSA]) and predicted by the investigator to need dialysis therapy within 10 weeks after the pre-screening period.
Subjects who, as judged by the investigator, are able to comprehend the pre-defined, standardized, modality education program and have undertaken this education during the screening period.
Subjects, or their legal representative, who, as judged by the investigator, are capable of being trained for home-based PD.
Subjects, or their legal representative, who are able to understand and voluntarily sign an ICF.
Subjects who are able to adhere to the study visit schedule and other protocol requirements.
Subjects who are able to regularly visit a HD center for HD therapy (≥ 3 times per week).
Subjects who, as judged by the investigator, are expected to remain on dialysis for at least 48 weeks.
Subjects who have normal liver function, as judged by the investigator.
Female subjects of childbearing potential who have a negative serum or urine pregnancy test at screening. Sexually active women of childbearing potential must agree to use adequate contraceptive methods, as judged by the investigator, while in the study.

Exclusion criteria

Subjects who are HIV positive.
Subjects who have already received a permanent PD catheter or HD access that is intended for permanent use before receiving modality education or have already received permanent dialysis. Subjects are not excluded if an access is present within 4 weeks before screening for back-up purposes or for acute treatment of life-threatening uremic symptoms, electrolyte abnormalities, or fluid overload.
Subjects who have a serious, uncontrolled medical disorder or active infection, which, as judged by the investigator, would jeopardize their ability to receive the prescribed dialysis treatment.
Subjects who have dementia or a mental status that would significantly affect the subject's understanding of the Informed Consent Form (ICF).
Subjects who are pregnant, intend to become pregnant during the study period, or are breast-feeding.
Subjects with a history of drug (defined as illicit drug use) or alcohol (defined as regular or daily consumption of more than 4 alcoholic drinks per day) abuse in the 2 years before screening.
Subjects who have previously received renal transplantation and are still being prescribed immunosuppressive therapy.
Subjects who are currently using or have used an investigational product within five half-lives of the physiological action or 30 days, whichever is longer, before screening.
Subjects who are unwilling or expected to be unable to fully comply with the visits and assessments required by the protocol.
Subjects who have previously been randomized in this study.
Subjects who are not eligible for either PD or HD, as judged by the investigator, due to:

PD: documented extensive intra-peritoneal adhesions or other condition contraindicated for PD.

HD: severe cardiac instability or other condition contraindicated for HD.
Subjects who have a serious or acute condition that, as judged by the investigator, would preclude participation in the study.
Subjects who have a malignancy requiring chemotherapy or radiation therapy.
Subjects undergoing temporary dialysis treatment between the screening visit and Day 1 that is expected to exceed 6 weeks in duration.
Subjects who have a life expectancy of less than 48 weeks.