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Pulmonary Embolism (Diagnosis)NCT07023705

MLPR As A Diagnostic Marker For Acute Pulmonary Embolism

An observational study of Pulmonary Embolism (Diagnosis) and Diagnosis, run by Ain Shams University at 1 site in Egypt.

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

A retrospective study to assess the utility of hematological marker (monocyte to large platelet ratio) to diagnose patients with pulmonary embolism Read more about this study

Who is it for?
Any age
Conditions the study is for
Pulmonary Embolism (Diagnosis), Diagnosis
What is being tested?
Monocyte to Large Platelet Ratio (MLPR)
How many people
53 participants
Where
1 siteEgypt
Study dates
1 Jan 2024to 31 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 Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patients presenting to the emergency department with signs and symptoms of pulmonary embolism who underwent CT pulmonary angiography for diagnosis.

Who may be able to join

  • Only patients with the results of full blood count and white blood cell differentiation, measured before the treatment of suspected PE.
  • Patients underwent CT pulmonary angiography to confirm or exclude pulmonary embolism diagnosis.

Who cannot join

  • Patient with history of any myeloproliferative disorder, myelofibrosis, Glanzmann thrombasthenia, May-Hegglin anomaly, Bernard-Soulier syndrome, suspicion of disseminated intravascular coagulation.
  • Patient receiving any anticoagulant drug at a therapeutic dose.
  • Patient with blood transfusion in the last 2 months.
  • Patients with acute coronary syndrome, pulmonary edema.
  • Patient on immunosuppressive drugs , Oral contraceptive pills .
  • Patients with severe renal or hepatic disease.
  • Patients with Stroke.
  • Patients with malignancy.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Ain Shams University

    Cairo

Other trials in Egypt

About this study

Official title: Monocyte To Large Platelet Ratio As A Diagnostic Marker For Acute Pulmonary Embolism

A retrospective study to assess the utility of hematological marker (monocyte to large platelet ratio) to diagnose patients with pulmonary embolism

Read the detailed description

The investigators conducted a retrospective review of emergency department records of patients who presented with signs and symptoms suggestive of pulmonary embolism (PE) and underwent CT pulmonary angiography (CTPA) for diagnosis. Hematological laboratory findings obtained prior to any treatment were collected and compared between two groups based on CTPA results: those with confirmed PE (CT positive) and those without PE (CT negative).

Being tested
Monocyte to Large Platelet Ratio (MLPR)
Medical subject headings
Pulmonary Embolism, Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Monocyte to Large Platelet Ratio (MLPR)Diagnostic test

    Admission laboratory values were used to calculate the Monocyte-to-Large Platelet Ratio (MLPR) by dividing the absolute monocyte count by the large platelet count. These values were obtained from blood samples collected before any treatment was administered.

Study groups in NCT07023705
Study groupRoleWhat they receive
Pulmonary embolismGroup that is confirmed to have pulmonary embolism by positive CTPA finding filling defect.
Receives: Diagnostic Test: Monocyte to Large Platelet Ratio (MLPR)
Non-Pulmonary embolismGroup that have pulmonary embolism diagnosis was excluded by negative CTPA finding.
Receives: Diagnostic Test: Monocyte to Large Platelet Ratio (MLPR)

What is being measured

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

  1. Monocyte-to-Large Platelet Ratio (MLPR)

    A ratio between monocyte absolute count and the large platelets count (MLPR) values compared between groups using Mann-Whitney U test; diagnostic accuracy evaluated by area under the curve (AUC) , sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV).

    Measured: At emergency department admission (baseline lab measurement) before any treatment.

Secondary outcomes (5)
  1. Mean platelet volume (MPV)

    MPV values compared between groups using Mann-Whitney U test; diagnostic accuracy evaluated by AUC, sensitivity, specificity, PPV, and NPV.

    Measured: At emergency department admission (baseline lab measurement) before any treatment.

  2. Neutrophil to Lymphocyte Ratio (NLR)

    The ratio between absolute neutrophil and absolute lymphocytes count (NLR) values compared between groups using Mann-Whitney U test; diagnostic accuracy evaluated by AUC, sensitivity, specificity, PPV, and NPV.

    Measured: At emergency department admission (baseline lab measurement) before any treatment.

  3. D-Dimer Levels

    D-Dimer concentration values compared between groups using Mann-Whitney U test; diagnostic accuracy evaluated by AUC, sensitivity, specificity, PPV, and NPV.

    Measured: At emergency department admission (baseline lab measurement) before any treatment.

  4. Platelet Distribution Width (PDW)

    PDW values compared between groups using Mann-Whitney U test; diagnostic accuracy evaluated by AUC, sensitivity, specificity, PPV, and NPV.

    Measured: At emergency department admission (baseline lab measurement) before any treatment.

  5. Platelet To Lymphocyte Ratio (PLR)

    The ratio between total platelets count and absolute lymphocytes count (PLR) values compared between groups using Mann-Whitney U test; diagnostic accuracy evaluated by AUC, sensitivity, specificity, PPV, and NPV.

    Measured: At emergency department admission (baseline lab measurement) before any treatment.

Timeline

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

  1. First posted17 Jun 2025
  2. Study start1 Jan 2024
  3. Primary completion31 Dec 2024
  4. Study completion31 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
Cohort
Time perspective
Retrospective
Enrolment
53 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07023705
Sponsor's protocol ID
FMASU MLPR 286
Status last verified
May 2026
First submitted
9 Jun 2025
Last updated
29 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Granger V, Faille D, Marani V, Noel B, Gallais Y, Szely N, Flament H, Pallardy M, Chollet-Martin S, de Chaisemartin L. Human blood monocytes are able to form extracellular traps. J Leukoc Biol. 2017 Sep;102(3):775-781. doi: 10.1189/jlb.3MA0916-411R. Epub 2017 May 2.

    PubMed 28465447
  • Moharamzadeh P, Rahmani F, Foroughifar S, Shahsavarinia K. Reliability of Platelet Indices for Diagnosing Pulmonary Embolism; a Brief Report. Adv J Emerg Med. 2019 Apr 28;3(3):e27. doi: 10.22114/ajem.v0i0.137. eCollection 2019 Summer.

    PubMed 31410404
  • Talay F, Ocak T, Alcelik A, Erkuran K, Akkaya A, Duran A, Demirhan A, Kar Kurt O, Asuk Z. A new diagnostic marker for acute pulmonary embolism in emergency department: mean platelet volume. Afr Health Sci. 2014 Mar;14(1):94-9. doi: 10.4314/ahs.v14i1.15.

    PubMed 26060464
  • Bialas AJ, Kornicki K, Ciebiada M, Antczak A, Sitarek P, Milkowska-Dymanowska J, Piotrowski WJ, Gorski P. Monocyte to large platelet ratio as a diagnostic tool for pulmonary embolism in patients with acute exacerbation of chronic obstructive pulmonary disease. Pol Arch Intern Med. 2018 Jan 31;128(1):15-23. doi: 10.20452/pamw.4141. Epub 2017 Nov 7.

    PubMed 29112185

Questions about this trial

What is this clinical trial studying?

An observational study of Pulmonary Embolism (Diagnosis) and Diagnosis, run by Ain Shams University at 1 site in Egypt.

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 2 inclusion and 8 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 29 May 2026. 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 Egypt. 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?

Monocyte-to-Large Platelet Ratio (MLPR) (time frame: At emergency department admission (baseline lab measurement) before any treatment.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07023705, which also lists 4 linked publications.

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 29 May 2026.

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