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A Study of Domestic Automated Peritoneal Dialysis Machine

Validity and Security of Domestic Automated Peritoneal Dialysis Machine: A Prospective, Randomized, Controlled, Multi-Center Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02388945
Enrollment
600
Registered
2015-03-17
Start date
2015-01-31
Completion date
2015-06-30
Last updated
2015-03-17

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

Conditions

Disorders Associated With Peritoneal Dialysis

Brief summary

This prospective, randomized, controlled, multi-center clinical trial will evaluate the validity and security of domestic APD machine compared with the patients followed CAPD.

Detailed description

Peritoneal dialysis (PD) is one of important way of renal replacement treatment worldwide. In China, about 40,000 patients suffered from end stage renal disease treated with PD, and almost of them followed continuous ambulatory peritoneal dialysis (CAPD) because of the expensive price of import automated PD (APD) machines although the higher clearance of solute, lower rate of PD related peritonitis and higher quality of life (QOL) in patients treated with APD compared those with CAPD. Now, cheaper domestic APD machines ( PDGO, Fuzhou, China) are accessed to the ESRD patients in china, but the efficacy and safety of which are not fully clear. This will be a prospective, randomized, controlled, multi-center study. Patients in treatment group will receive APD while those in control group will receive CAPD for 8 weeks. After followed-up for 8 weeks, the adequacy of PD, residual kidney function , peritoneum function and QOL of patients will be evaluated.

Interventions

OTHERAPD

PDGO APD machines used in the PD patients for 8 weeks

OTHERCAPD

CAPD used in the PD Patients for 8 weeks

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. The duration of PD is more than 1 month. 2. The age is range from 18 to 80 years old. 3. The patient can be treated with regular PD in home. 4. The volume of peritoneal dialysate is from 8L to 10 L in 1 day. 5. The patient can be visited regularly. 6. The patient must be freely given informed consent

Exclusion criteria

1. Peritonitis was happened within 1 month 2. The KT/V\<1.7 3. Infections in the exit or tunnel 4. With tumors. 5. With low transport of peritoneum. 6. With mental and behavior disorders. 7. With acute renal failure 8. Hemodialysis meanwhile 9. With heart failure( NYHA III-IV ) or cardio- cerebrovascular events 10. Attending other clinical trails 11. Refused to give informed consent Exit criteria (1)Stop PD for more than 10 days (2)The patient demand to quit from the RCT (3)With serious adverse events.

Design outcomes

Primary

MeasureTime frameDescription
Adequacy of dialysisup to 8 weekskt/v

Secondary

MeasureTime frameDescription
Residual kidney functionup to 6 monthsResidual kidney kt/v
Peritoneal functionup to 6 monthsPeritoneal equilibration test

Countries

China

Contacts

Primary ContactZongpei Jiang, M.D. & Ph.D.
jx.home@medmail.com.cn8620-38379727

Outcome results

None listed

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