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Completed Phase 4 Interventional Results available

Octaplas Pediatric Plasma Exchange Trial

ClinicalTrials.gov ID: NCT01938378

Public ClinicalTrials.gov record NCT01938378. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 9:52 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label, Multicenter, Post-Marketing Requirement Study to Investigate the Safety and Tolerability of Octaplas™ in the Management of Pediatric Patients Who Require Therapeutic Plasma Exchange

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To assess the safety and tolerability of octaplas™ in the pediatric population by monitoring serious adverse drug reactions, adverse drug reactions (ADRs), thrombotic events (TEs), thromboembolic events (TEEs) and by measuring safety laboratory parameters in pediatric patients who require therapeutic plasma exchange.

Study identification

NCT ID
NCT01938378
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Octapharma
Industry
Enrollment
41 participants

Conditions and interventions

Eligibility (public fields only)

Age range
2 Years to 20 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2015 (Type not available)
Primary completion
Jan 27, 2019 (Actual)
Completion
Jan 27, 2019 (Actual)
Last update posted
Mar 24, 2020

2015 – 2019

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
Octapharma Research Site Birmingham Alabama 35233 —
Octapharma Research Site Atlanta Georgia 30322 —
Octapharma Research Site New Orleans Louisiana 70118 —
Octapharma Research Site Minneapolis Minnesota 55455 —
Octapharma Research Site Kansas City Missouri 64108 —
Octapharma Research Site St Louis Missouri 63130 —
Octapharma Research Site Durham North Carolina 27710 —
Octapharma Research Site Cincinnati Ohio 45229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01938378, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 24, 2020 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01938378 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →