NCT05092724

Brief Summary

In December 2019, a sudden public health incident (the corona virus disease \[COVID-19\] epidemic) occurred in Wuhan, China. Clinical features of those with pneumonia include fever and cough, and in many cases a sudden and accelerating respiratory distress originated from interstitial pneumonia . Many hypotheses have explained hypoxemia in COVID-19 patients, such as hyperimmune reaction to viral infection and cytokine storm that leads to serious lung tissue and alveolar damage or even direct viral insult . Mortality are as high as 15% in critically ill patients requiring intensive care unit admission and oxygen therapy , suggesting an urgent need to try therapeutic interventions in addition to supportive treatment. There is more than one type of hemoglobin. In adults, Hb A or Adult hemoglobin which is the main hemoglobin in the blood. But there is another type of hemoglobin called fetal hemoglobin. Fetal hemoglobin (hemoglobin F, Hb F, or α2γ2) is the main oxygen carrier protein in the human fetus. and the levels remain high after birth until the baby is roughly 2-4 months old . Hemoglobin F has a different composition from hemoglobin A and higher affinity to oxygen . At birth, hemoglobin F accounts for 50-95% of the infant's hemoglobin and at around 6 months after birth, hemoglobin A becomes the predominant type.The key feature that allows hemoglobin F to bind more strongly to oxygen is by having γ subunits (instead of β, in Hb A for example). 2,3-BPG interacts much more with hemoglobin A than hemoglobin F . A hypothesis for the low incidence of the COVID-19 infection in pediatric is the presence of fetal hemoglobin (HbF) . In a preliminary study about the prevalence of hemoglobinopathies in different countries and the mortality rate of COVID-19, it appears that the mortality is lower in countries with a higher prevalence of hemoglobinopathies . Mice treated with GBT1118 (a compound that enhances the oxygen affinity of hemoglobin) showed a sustained significant increase in SpO2 over 4 h of hypoxia exposure. People with haemoglobinopathies like sickle cell anemia or beta-thalassemia attributed with high amount of fetal hemoglobin, become mostly asymptomatic or have mild symptoms . The volume of umbilical cord blood varies from 50 ml to 140 ml with a mean of 85 ml rich in fetal hemoglobin . Mesenchymal stem cells (MSCs) have been widely used in the clinical setting, not only for autoimmune diseases but also for infectious diseases , and their safety and effectiveness have been well elucidated . As a noninvasive treatment, hUC-MSC therapy is a very effective and promising method for clinical application and promotion to treat severe COVID-19 the investigators offer a solution by increasing fetal hemoglobin by cord blood containing fetal blood transfusion in the critical patients as a trial to combat the course of the disease and minimize the morbidity especially in sever cases who suffer from desaturation until suppression of the immune dysregulation and avoidance of the impending death.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Dec 2021

Shorter than P25 for not_applicable

Status
unknown

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

October 19, 2021

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 25, 2021

Completed
1 month until next milestone

Study Start

First participant enrolled

December 1, 2021

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 19, 2022

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2022

Completed
Last Updated

November 23, 2021

Status Verified

November 1, 2021

Enrollment Period

3 months

First QC Date

October 19, 2021

Last Update Submit

November 20, 2021

Conditions

Outcome Measures

Primary Outcomes (1)

  • • To evaluate the effect of increasing fetal hemoglobin protocol on the outcome in patients with fulminant COVID-19

    To show how fetal blood transfusion (cord blood ) improve the outcome of COVID 19 patient ( mortality)

    for 10 cases for each group ( pilot study ) allover about 5 months

Secondary Outcomes (1)

  • To evaluate the effect of increasing fetal hemoglobin protocol on the morbidity of patients with fulminant COVID-19

    allove 5 months . 10 days for each group .

Study Arms (2)

standard protocol of manaegement

NO INTERVENTION

fetal blood

ACTIVE COMPARATOR
Procedure: fetal blood transfusion

Interventions

transfusion of fetal blood

fetal blood

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Admitted covid 19 patients to the ICU with the following criteria : :
  • Hypoxia (P/F less than 100)
  • Need for high level of oxygenation or ventilatory support
  • Tachypnea, respiratory distress due to hypoxia
  • \>50 percent involvement of the lung parenchyma on chest imaging .
  • Serum IL-6 ≥ 5 x upper normal limit of daily increase of \>1 time
  • Ferritin \>300 ug/L with doubling within 24 hours
  • Ferritin \>600 ug/L at presentation
  • LDH \>250 U/L
  • Elevated D-dimer (\>1 mg/L)

You may not qualify if:

  • Patients with hemodynamic instability or multiorgan failure 2- Failure to obtain temporary vascular access under ultrasound guidance or due to bleeding tendency.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Blood Transfusion, Intrauterine

Intervention Hierarchy (Ancestors)

Blood TransfusionBiological TherapyTherapeuticsFetal Therapies

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

October 19, 2021

First Posted

October 25, 2021

Study Start

December 1, 2021

Primary Completion

February 19, 2022

Study Completion

March 31, 2022

Last Updated

November 23, 2021

Record last verified: 2021-11