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NCT00406536 · ClinicalTrials.gov registry record · Phase 2

Study of LYM-X-SORB™ to Improve Fatty Acid and Choline Status in Children With CF and PI

A Phase 2 study of Cystic Fibrosis and Pancreatic Insufficiency, sponsored by Avanti Polar Lipids.

Completed
Registry status
Phase 2
Development phase
110
Enrollment target
1
Study location

NCT00406536 is a Phase 2 study of Cystic Fibrosis and Pancreatic Insufficiency that has completed, run by Avanti Polar Lipids. The registered enrollment target is 110 participants, below the 179-participant average among 169 other Cystic Fibrosis trials with a reported enrollment target (39% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00406536, a Phase 2 study of Cystic Fibrosis and Pancreatic Insufficiency, has completed, sponsored by Avanti Polar Lipids.

COMPLETED
Registry status
Phase 2
Development phase
110 participants
Enrollment target
1
Study location

Study Summary

The purpose of this phase II research study is to evaluate the effectiveness of the next generation LYM-X-SORB™ in improving the essential fatty acid (EFA) and choline status for children and adolescents with Cystic Fibrosis (CF) and pancreatic insufficiency (PI).

Interventions

  • DIETARY_SUPPLEMENT Lym-X-Sorb powder
  • DIETARY_SUPPLEMENT Placebo powder

Study Locations (1)

Pennsylvania

  • Children's Hospital of Philadelphia (CHOP) - Philadelphia

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2007-01
Est. Completion 2012-06
Phase Phase 2

Sponsor

Avanti Polar Lipids

1 total trials

What the Registry Record Tells You About NCT00406536

The ClinicalTrials.gov registry entry for NCT00406536 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 179-participant average among 169 other Cystic Fibrosis trials with a reported enrollment target (39% lower). The listed sponsor is Avanti Polar Lipids, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Cystic Fibrosis appearing as the primary indexed condition, and to 2 interventions - of which Lym-X-Sorb powder is the first listed.

NCT00406536 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00406536 about?

NCT00406536 is a clinical study titled "Study of LYM-X-SORB™ to Improve Fatty Acid and Choline Status in Children With CF and PI". The purpose of this phase II research study is to evaluate the effectiveness of the next generation LYM-X-SORB™ in improving the essential fatty acid (EFA) and choline status for children and adolescents with Cystic Fibrosis (CF) and pancreatic insufficiency (PI).

What is the current status of trial NCT00406536?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 110 participants. The study started on 2007-01. Estimated completion is 2012-06.

What conditions does trial NCT00406536 study?

This clinical trial studies the following conditions: Cystic Fibrosis, Pancreatic Insufficiency.

What interventions are being tested in trial NCT00406536?

The interventions under investigation include: Lym-X-Sorb powder (DIETARY_SUPPLEMENT), Placebo powder (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT00406536?

This trial is sponsored by Avanti Polar Lipids, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00406536 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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