- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04064801
Red Cell Distribution Width as a Predictor of Mortality in Acute Methanol Poisoning
April 12, 2021 updated by: Barış Arslan, Adana Numune Training and Research Hospital
The study aimed to investigate the association between RDW and in-hospital mortality in methanol poisoning.
Study Overview
Status
Completed
Conditions
Detailed Description
RDW values have been found to be an independent predictor of the prognosis among patients with heart diseases, stroke,community-acquired pneumonia (CAP), pulmonary embolism, chronic obstructive pulmonary disease (COPD), septic shock, and acute pancreatitis.
Study Type
Observational
Enrollment (Actual)
42
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Adana, Turkey, 01170
- Adana City Training and Research Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with acute methanol toxicity who were diagnosed and treated at the Adana City Training and Research Hospital
Description
Inclusion Criteria:
All patients aged ≥18 years who were admitted to emergency departments from January 2019 to January 2020 on account of acute methanol intoxication.
Exclusion Criteria:
Incomplete data, Malignancy, Severe anaemia, History of erythrocyte transfusion last 6 weeks
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Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Hospital mortality
Time Frame: 7 day
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7 day
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Need for mechanical ventilation
Time Frame: 7 day
|
7 day
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
March 15, 2020
Primary Completion (ACTUAL)
May 30, 2020
Study Completion (ACTUAL)
August 30, 2020
Study Registration Dates
First Submitted
August 20, 2019
First Submitted That Met QC Criteria
August 20, 2019
First Posted (ACTUAL)
August 22, 2019
Study Record Updates
Last Update Posted (ACTUAL)
April 15, 2021
Last Update Submitted That Met QC Criteria
April 12, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AdanaCTYHOSP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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