NCT04335955

Brief Summary

Platelets (PLT), a major and essential constituent of blood, plays an important role in physiological and pathological processes such as coagulation, thrombosis, inflammation and maintenance of vascular endothelial cells the integrity (1). Platelet indices are a group of parameters that are used to measure the total amount of PLTs, PLTs morphology and proliferation kinetics (2). The commonly used PLT indices include PLT count, mean platelet volume (MPV), platelet distribution width (PDW), and plateletcrit (PCT). The MPV refers to the ratio of PCT to PLT count. PDW is numerically equal to the coefficient of PLT volume variation, which is used to describe the dispersion of PLTs volume (3). It is well known that platelet indices have been applied in the diagnosis of hematological system diseases. In recent years, it has been discovered that these indices are related to the severity of illness and patients' prognosis. Reduction in PLT count is an independent risk factor for critically ill patients in intensive care unit (4). In addition, Acute Physiology and Chronic Health Evaluation II (APACHE II) System also includes thrombocytopenia as an independent risk factor for mortality (5). In a recent research, it will be reported that MPV will be rising with interleukin-6 and C-reactive protein in septic premature infants. MPV has been used as predictor of many inflammatory diseases as MPV significantly higher on both day 1 and day 3 in neonatal sepsis (6). In addition, in patients with cirrhosis and ascites, elevated PDW and MPV will be accurate diagnostic predictors for ascetic fluid infection (7). MPV and PDW will be used as biomarkers predicting the development of postoperative sepsis in colorectal cancer patient (8). All these evidences indicated that PLT indices will be considered as indicator in a series of diseases (9). Advantages of platelet indices are simple, available, cheap tools and routinely done in the hospital laboratory in all critical ill patients and may be a useful, sensitive tool for diagnosis and monitoring these patients especially in limited resource countries as Egypt. However, whether PLT indices are correlated with procalcitonin in assessment the severity of illness is still under research in septic patients

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
54

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2020

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 3, 2020

Completed
4 days until next milestone

First Posted

Study publicly available on registry

April 7, 2020

Completed
24 days until next milestone

Study Start

First participant enrolled

May 1, 2020

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2020

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2020

Completed
Last Updated

November 24, 2023

Status Verified

November 1, 2023

Enrollment Period

6 months

First QC Date

April 3, 2020

Last Update Submit

November 22, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • The correlation between platelet indices and 30 days mortality among critically ill septic patients

    The correlation between platelet indices and 30 days mortality among critically ill septic patients

    within 30 days from hospital admission

Secondary Outcomes (3)

  • Correlation between platelet indices and Length of ICU stay (days)

    within 30 days from hospital admission

  • Correlation between platelet indices and detection of organs dysfunction

    within 30 days from hospital admission

  • Correlation between platelet indices and procalcitonin.

    within 30 days from hospital admission

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Sepsis: life-threatening organ dysfunction caused by a dysregulated host response to infection. According to the 2016 consensus definitions, an increase in SOFA score of 2 or more constitutes organ dysfunction

You may qualify if:

  • patients aged 18-65 years ICU stay more than 24 hours septic patients according to Third International Consensus Definitions Septic Shock patients according to Third International Consensus Definitions

You may not qualify if:

  • Pregnant women
  • Patients with active hemorrhage
  • Patients with hematological diseases (including anemia, hypersplenism
  • Lymphoma or leukemia
  • Rheumatism, and bone marrow diseases)
  • Patients who had infused with blood or platelets prior to their admission
  • Patients who had used anti-platelet drugs prior to their admission
  • Patients who had received radiotherapy or chemotherapy or bone marrow transplantation 1 month prior to admission.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Amany Afheem

Tanta, Egypt

Location

MeSH Terms

Conditions

Sepsis

Condition Hierarchy (Ancestors)

InfectionsSystemic Inflammatory Response SyndromeInflammationPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
sponsor investigator

Study Record Dates

First Submitted

April 3, 2020

First Posted

April 7, 2020

Study Start

May 1, 2020

Primary Completion

October 31, 2020

Study Completion

November 30, 2020

Last Updated

November 24, 2023

Record last verified: 2023-11

Locations