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HLHNEHRNCT07800234

Establishing a National Egyptian HLH Registry (NEHR)

An observational study of HLH and Hemophagocytic Lymphohistiocytoses, run by Ain Shams University at 2 sites in Egypt.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Establishing a National Egyptian HLH Registry (NEHR) Read more about this study

Who is it for?
Ages Up to 18 years
Conditions the study is for
HLH, Hemophagocytic Lymphohistiocytoses
How many people
100 participants
Where
2 sitesEgypt
Study dates
2 Mar 2024to 1 Dec 2028
Phase
Observational
Are there results?
Not yet: the study is under way

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 Up to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Study population: Patients diagnosed with hlh

Who may be able to join

  • patients diagnosed with hlh

Who cannot join

  • adults

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Iman Ragab Prof of Pediatrics, Ain Shams University, Professor contact

+20 1002550680

hragab68@hotmail.com

Fatma Ebeid Professor of pediatrics, Ain Shams University, Professor contact

+201095569596

Egypt2 sites, 1 recruiting
  • Faculty of Medicine Pediatric Hematology Oncology Department

    Cairo, 11566

    Iman Ragab Professor of Pediatrics, MD, +201095569596, hragab68@hotmail.com

    Fatma Soliman Elsayed Ebeid Professor of Pediatrics, MD, +201095569596, fatmaebeid@med.asu.edu.eg

    Recruiting
  • Faculty of medicine ain shams university

    Cairo

    Active, not recruiting

Other trials in Egypt

About this study

Establishing a National Egyptian HLH Registry (NEHR)

Medical subject headings
Lymphohistiocytosis, Hemophagocytic

What participants receive

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

Study groups in NCT07800234
Study groupRoleWhat they receive
Hemophagocytic lymphohistiocytosis (HLH)Children diagnosed with Hemophagocytic lymphohistiocytosis (HLH)

What is being measured

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

  1. A nationwide HLH map

    Establish a nationwide map for children with presumed diagnosis of HLH

    Measured: 2 years

Timeline

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

  1. First posted2 Sep 2026
  2. Study start2 Mar 2024
  3. Primary completion1 Jan 2028 (estimated)
  4. Study completion1 Dec 2028 (estimated)

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
Other
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07800234
Sponsor's protocol ID
FMASU P05/2024
Acronym
NEHR
Status last verified
Aug 2026
First submitted
30 Aug 2026
Last updated
2 Sep 2026
Results posted
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 HLH and Hemophagocytic Lymphohistiocytoses, run by Ain Shams University at 2 sites 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 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: looking for participants now, as of the sponsor's last update on 2 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Iman Ragab Prof of Pediatrics, Ain Shams University, Professor (+20 1002550680, hragab68@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

A nationwide HLH map (time frame: 2 years). 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 2 Sep 2026.

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