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Methanol PoisoningNCT04064801

Red Cell Distribution Width as a Predictor of Mortality in Acute Methanol Poisoning

An observational study of Methanol Poisoning, run by Adana Numune Training and Research Hospital at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study aimed to investigate the association between RDW and in-hospital mortality in methanol poisoning. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Methanol Poisoning
How many people
42 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Mar 2020to 30 Aug 2020
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with acute methanol toxicity who were diagnosed and treated at the Adana City Training and Research Hospital

Who may be able to join

  • All patients aged ≥18 years who were admitted to emergency departments from January 2019 to January 2020 on account of acute methanol intoxication.

Who cannot join

  • Incomplete data, Malignancy, Severe anaemia, History of erythrocyte transfusion last 6 weeks
  • -

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Adana City Training and Research Hospital

    Adana, 01170

Other trials in Turkey (Türkiye)

About this study

The study aimed to investigate the association between RDW and in-hospital mortality in methanol poisoning.

Read the 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.

Keywords
Alcohol, red blood cell distribution width, methanol poisoning, prognosis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Hospital mortality

    Measured: 7 day

  2. Need for mechanical ventilation

    Measured: 7 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Aug 2019
  2. Study start15 Mar 2020
  3. Primary completion30 May 2020
  4. Study completion30 Aug 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
42 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04064801
Sponsor's protocol ID
AdanaCTYHOSP
Status last verified
Apr 2021
First submitted
20 Aug 2019
Last updated
15 Apr 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Methanol Poisoning, run by Adana Numune Training and Research Hospital at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Apr 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Hospital mortality (time frame: 7 day). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Apr 2021.

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