Menu
Not yet recruiting NCT06988826

Comparison of G-CSF & Antibiotics Versus Antibiotics Alone in Resolution of Febrile Neutropenia

Phase IV Interventional Febrile Neutropenia Febrile Neutropenia, Rule of Clinical Decision, Chemotherapy Febrile Neutropenia, Drug-Induced G-CSF

For patients and families

In plain language

Fill the application

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: G-CSF, Antibiotics only.
Who it may be relevant to
Registry conditions: Febrile Neutropenia, Febrile Neutropenia, Rule of Clinical Decision, Chemotherapy, Febrile Neutropenia, Drug-Induced, G-CSF. Basic parameters: 1 year — 16 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of Antibiotics With and Without Granulocyte Colony-Stimulating Factor in Children With Chemotherapy Induced Febrile Neutropenia

Overview

This study aim to find the best option for children having cancer who develop low immunity state due to chemotherapy

Detailed description

Children having a cancer diagnosis and treated with chemotherapy often develop neutropenia. This creates an immunocompromised state which can result in infections manifested by fever. This study compares two treatment options to find out the best treatment for these patients.

Interventions

  • Drug G-CSF
    G-CSF \& Antibiotic therapy in combination
  • Drug Antibiotics only
    Antibiotics alone

Primary outcome measures

  • Resolution of FN [Time frame: 2 weeks]
Secondary outcome measures (2)
  • Afebrile [Time frame: 2 weeks]
  • Length of hospital stay [Time frame: 2 weeks]

Eligibility criteria

Inclusion criteria

  • Age 1-16 years
  • any Gender
  • Febrile neutropenia
  • diagnosed case of solid or hematological malignancy
  • taking chemotherapy

Exclusion criteria

  • Non-neutropenic fever
  • already received G-CSF or antibiotics before presenting to hospital
  • any other cause of neutropenia

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06988826 · 656/CH-UCHS/15/5/2023

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗