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NCT01202708 · ClinicalTrials.gov registry record · NA

Gambro AK200 ULTRA Hemodiafiltration Study

A NA study of Chronic Renal Failure, sponsored by Vantive Health.

Completed
Registry status
NA
Development phase
14
Enrollment target
1
Study location

NCT01202708: Completed NA study of Chronic Renal Failure, sponsored by Vantive Health.

NCT01202708 is a NA study of Chronic Renal Failure that has completed, run by Vantive Health. The registered enrollment target is 14 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01202708, a NA study of Chronic Renal Failure, has completed, sponsored by Vantive Health.

COMPLETED
Registry status
NA
Development phase
14 participants
Enrollment target
1
Study location

Study Summary

This study is designed to assess the safety, efficacy and dialytic capabilities of hemodiafiltration with on-line prepared substitution fluid using the AK200 ULTRA in comparison to conventional hemodialysis.

Conditions Studied

Interventions

  • DEVICE On line hemofiafiltration
  • DEVICE On line hemodiafiltration

Study Locations (1)

District of Columbia

  • George Washington University Medical Center - Washington D.C.

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 1997-08
Phase NA
Vantive Health

15 total trials

What the finished NCT01202708 record still lists

NCT01202708 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Chronic Renal Failure appearing as the primary indexed condition, and to 2 interventions - of which On line hemofiafiltration is the first listed.

NCT01202708 reports a single indexed study location in District of Columbia.

Frequently Asked Questions

What is clinical trial NCT01202708 about?

NCT01202708 is a clinical study titled "Gambro AK200 ULTRA Hemodiafiltration Study". This study is designed to assess the safety, efficacy and dialytic capabilities of hemodiafiltration with on-line prepared substitution fluid using the AK200 ULTRA in comparison to conventional hemodialysis.

What is the current status of trial NCT01202708?

This trial is currently completed. It is a NA study. The enrollment target is 14 participants. The study started on 1997-08.

What conditions does trial NCT01202708 study?

This clinical trial studies the following conditions: Chronic Renal Failure.

What interventions are being tested in trial NCT01202708?

The interventions under investigation include: On line hemofiafiltration (DEVICE), On line hemodiafiltration (DEVICE).

Who is sponsoring clinical trial NCT01202708?

This trial is sponsored by Vantive Health, which has 15 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01202708 being conducted?

This trial has 1 study location across District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Chronic Renal Failure

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01202708's enrollment target sits among peer trials

14 1909th of 2000 higher than 90 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01202708, the US trial registry maintained by the National Library of Medicine. NCT01202708 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.