Status:

UNKNOWN

Initial Hemopurification Strategy for Acute Paraquat Poisoning in Adults

Lead Sponsor:

Peking Union Medical College Hospital

Collaborating Sponsors:

The First Affiliated Hospital of Zhengzhou University

National Natural Science Foundation of China

Conditions:

Poisoning

Eligibility:

All Genders

18-70 years

Phase:

NA

Brief Summary

HeSAPP is a single-center, non-blinded, parallel-group randomized controlled trial studying the hemopurification strategy for acute paraquat(PQ) poisoned patients. The intervention to be investigated ...

Detailed Description

Patients diagnosed with acute paraquat poisoning in the Emergency Room of the First Affiliated Hospital of Zhengzhou University would be stratified according to their urine dithionite test results and...

Eligibility Criteria

Inclusion

  • Suspected paraquat ingestion history (intended or accidental), which is confirmed by positive urine dithionite result (light blue, navy blue and dark blue).
  • Arriving at the ER within 24 hours after PQ digestion.
  • No known current pregnancy or lactation.
  • Absence of cardiac arrest after poisoning, and no previous or present history of chronic kidney disease, chronic liver disease, respiratory failure, COPD, asthma, heart failure, pancreatic disease, acute coronary syndrome (ACS) or stoke.
  • No known combined ingestion with other poisons or alcohol.
  • No previous blood purification treatment prior to admission.
  • No known participation in other medical trials.
  • Agreement on informed consent.

Exclusion

  • Patients who are unable to comply with the procedures of the present trial, including those who change therapy or withdraw treatment.
  • Patients who develop severe allergic response to HP materials.
  • Patients who do not receive intervention within 4 hours after admission in reality.

Key Trial Info

Start Date :

October 1 2018

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

February 28 2022

Estimated Enrollment :

360 Patients enrolled

Trial Details

Trial ID

NCT03314909

Start Date

October 1 2018

End Date

February 28 2022

Last Update

April 17 2018

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