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RecruitingNCT07374185bone marrowUpdated Sep 15, 2026

Using Autologous Bone Marrow Cells With Wharton Gel Exosomes to Stimulate Hepatic Cell Repair in Liver Cirrhosis

An interventional study of Autologous Bone Marrow Aspirate Concentrate in Liver Cirrhosis, sponsored by Global Stem Cell Center, Baghdad. Recruiting at 1 site in Iraq. Open to participants aged Up to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-15.

Sponsored by Global Stem Cell Center, Baghdad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Feb 2026; still recruiting 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
Up to 80 Years
Sex
All
01

Study summary

the study includes patients with liver cirrhosis irrespective of the stage excluding people with active tumor or other major health issue endangering life, the protocol includes the use of autologous bone marrow derived mononuclear cells harvested from the same patient under local anesthesia ,followed by cell concentration and viability testing , then final product is combined with small volume of 2 cc of Wharton gel exosomes 20 billion per to be administered intravenously.

Read the detailed description

Mesenchymal stem cell therapy is one option that can help in improving liver functions if given parenteral, those mesenchymal stem cells can be harvested from different sources ,regarding this trial investigators use bone marrow derived mononuclear cells taken from posterior crest of iliac bone of the same patient, the bone marrow volume taken is around 50 cubic milliliter to be followed by filtration to get rid of bone fragments then Wharton gel exosomes are added in 2 cc volume and total 20 billion particles ,the product is administered intravenously .

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Conditions studied

  • Liver Cirrhosis

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03

In context

Liver Cirrhosis

1,298 studies on the registry are indexed under Liver Cirrhosis; 338 are open to participants now.

This study's planned enrollment of 10 is below the median of 78 across 739 interventional studies indexed under Liver Cirrhosis.

Browse Liver Cirrhosis studies →

Lead sponsor

Global Stem Cell Center, Baghdad is the lead sponsor of 3 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Up to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria: any patient with liver cirrhosis , less than 80 years of age -

Exclusion Criteria:

  1. active .
  2. severe sepsis.
  3. pregnancy. -
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Active comparator
    active treatment cellular product arm

    autologous bone marrow aspiration is done under sedation with the addition of Wharton gel 2 cc exosomes then given intravenously after using 170 micron filter.

    Procedure: Autologous Bone Marrow Aspirate Concentrate

Interventions

  • ProcedureAutologous Bone Marrow Aspirate Concentrate

    using autologous bone marrow aspirated from iliac crest ,centrifuged and then injected intravenously

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What researchers measure

Primary outcomes

  1. child-Pugh score for liver cirrhosis

    The Child-Pugh score is a clinical tool used to assess the severity and prognosis of chronic liver disease, especially cirrhosis, by evaluating five key factors: total bilirubin, albumin, INR (prothrombin time), ascites, and hepatic encephalopathy, with each getting 1-3 points (1=best, 3=worst). Summing these points categorizes patients into Class A (5-6 points, well-compensated), B (7-9 points, moderately impaired), or C (10-15 points, severe dysfunction), helping guide treatment, predict surgical risk, and manage liver transplant needs. A is minimum and C maximum

    Time frame: 12 weeks up to 12 months

  2. child-Pugh score of 3 stages depends on bilirubin level, serum albumin ,prothrombin time ,ascites ,encephalopathy

    measurement of prothrombin time, albumin, serum bilirubin level and assess ascites and hepatic encephalopathy

    Time frame: 12 months

07

Study locations

1 of 1 sites recruiting
  • Capital Private Hospital Alrabee Street
    Baghdad, Iraq 964, Iraq
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07374185
Lead sponsor
Global Stem Cell Center, Baghdad
Responsible party
Sponsor
First posted
Jan 28, 2026
Start date
Feb 20, 2026
Primary completion
Dec 20, 2026 (estimated)
Completion
Dec 20, 2026 (estimated)
Last update
Sep 15, 2026

Study contacts

abdulmajeed hammadi
Contact
hammadimajeed@gmail.com
+9647902268105
khalil juma kareem kareem
Contact
hammadimajeed@gmail.com
+9647803977072

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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