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Pulmonary Embolism (PE)NCT07009301

Pulmonary Embolism Following Viper's Bites: A Case Report

An observational study of Pulmonary Embolism (PE) and Snake Envenomation, run by Younes Oujidi at 1 site in Morocco.

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

Viper envenomation constitutes a medical emergency predominantly occurring in rural regions, where specific viper species are endemic, with their distribution influenced by climatic variations. Read more about this study

Who is it for?
Ages 18 to 100 years, women only
Conditions the study is for
Pulmonary Embolism (PE), Snake Envenomation
How many people
1 participants
Where
1 siteMorocco
Study dates
10 Jan 2025to 20 May 2025
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 to 100 years
  • Women only
  • Adult, Older adult

Study population: People aged above 18years, developing a pulmonary embolism after snake bites

Who may be able to join

  • Age above 18years old

Who cannot join

  • Not bitten by snakes

Trial locations and contacts

1 site in 1 country.

Morocco1 site
  • University hospital center Mohammed VI of Oujda

    Oujda

Other trials in Morocco

About this study

Official title: An Observational Study About a Case of Pulmonary Embolism Following Viper's Bite

Viper envenomation constitutes a medical emergency predominantly occurring in rural regions, where specific viper species are endemic, with their distribution influenced by climatic variations. The literature describes numerous complications associated with viper bites, including neurological disturbance, hematological abnormalities, and irreversible renal failure.

We report the case of a 65-year-old female patient admitted to the intensive care unit for viper envenomation characterized by extensive local edema. Diagnostic investigations, including laboratory tests and imaging studies, revealed the presence of a bilateral pulmonary embolism. The patient was subsequently treated with antivenom therapy, followed by initiation of low molecular weight heparin. Despite the recognized high risk of viper envenomation described in the literature, the patient experienced an uncomplicated clinical course and was discharged in stable condition with no further complications.

Medical subject headings
Pulmonary Embolism, Snake Bites

What is being measured

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

  1. Evolution of hematological blood test during the ICU stay

    Measured: From January 2025 to May 2025

Timeline

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

  1. First posted6 Jun 2025
  2. Study start10 Jan 2025
  3. Primary completion25 Jan 2025
  4. Study completion20 May 2025

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
Case only
Time perspective
Retrospective
Enrolment
1 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07009301
Sponsor's protocol ID
Critial Care
Status last verified
May 2025
First submitted
29 May 2025
Last updated
6 Jun 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Pulmonary Embolism (PE) and Snake Envenomation, run by Younes Oujidi at 1 site in Morocco.

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 1 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 6 Jun 2025. 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 Morocco. 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?

Evolution of hematological blood test during the ICU stay (time frame: From January 2025 to May 2025). 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 6 Jun 2025.

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