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Extraordinary Measures for Egyptian Children With Hemato-Oncological Disorders During COVID-19 Pandemic (PedCan-COVID)

F

Fatma Soliman Elsayed Ebeid, MD

Status

Completed

Conditions

Coronavirus COVID-19

Study type

Observational

Funder types

Other

Identifiers

NCT04404244
FMASU P25a/ 2020

Details and patient eligibility

About

This is a prospective follow-up non-intervention study that will be carried out at Hematology/ Oncology Department, Children's hospital, Ain-Shams University, Cairo, Egypt. All followed-up children below 18 years with cancer during the one year study period from May 2020 till Apr 2021 either at the out-patients clinic or inpatient department will be recruited.

Full description

Study Procedures:

On admission or during the outpatient visit:

  1. Obtaining an informed consent .
  2. Full medical history, concurrent medications, demographic data and epidemiological data (history of contact to a COVID-19 case, history of travel), will be obtained.
  3. A thorough physical examination will be performed.
  4. Body weight, height, BMI, vital signs (blood pressure, heart rate and temperature) and blood oxygen saturation) will be recorded.
  5. Laboratory to perform the following tests:

Complete blood count with differential counts, COVID -19 reverse Transcription Polymerase Chain Reaction (RT-PCR) test by nasopharyngeal swab.

During admission:

Whenever unexplained fever and or respiratory symptoms developed or whenever COVID19 suspected to have the following to be performed:

  1. Symptom developed that necessitates to repeat oropharyngeal and nasopharyngeal swab if indicated will be collected
  2. Chest X-ray or CT chest will be recorded.
  3. Laboratory to perform the following tests:

Complete blood count with differential counts,

COVID-19 RT-PCR test by oropharyngeal and nasopharyngeal swab:

C-reactive protein and serum ferritin level. Coagulation test; D. dimer, prothrombin time and INR. Routine bacteriological study, blood culture and other symptoms/signs based cultures will be recorded

On discharge:

  • Date of discharge
  • Period of admission
  • Period of fever
  • A thorough physical examination will be performed
  • Record the outcome

Enrollment

800 patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Children below 18 years with malignancy either hematological or solid tumors or
  2. Children below 18 years with hematological condition

Exclusion criteria

  1. Patients or care-givers refusal to be enrolled in the study

Trial contacts and locations

1

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Central trial contact

Fatma Ebeid

Data sourced from clinicaltrials.gov

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