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CompletedNCT06302543alfarahUpdated Sep 14, 2026

Treatment of Premature Ovarian Insufficiency Using Bone Marrow Cells

An interventional study of autologous bone marrow cells injection in Premature Ovarian Insufficiency, sponsored by abdulmajeed hammadi. Completed at 1 site in Iraq. Open to female participants aged 30 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-14.

Sponsored by abdulmajeed hammadi · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
30 Years to 60 Years
Sex
Female
01

Study summary

investigator is doing single armed clinical interventional study to treat premature ovarian insufficiency with autologous bone marrow derived mononuclear cells to be given systematically and locally to the ovaries under ultrasound guidance with experienced gynecologist and to look for the results including: laboratory evidence through hormonal study ultrasound proof of ovarian follicle development. premature ovarian insufficiency is characterized by early loss of ovarian function (less than 40 years of age) manifested by menstrual irregularity or amenorrhea with elevated levels of gonadotropin hormones and low estrogen and anti-Mullerian hormone.

Autologous use of stem cells from bone marrow are alternative safe minimal manipulative products that can provide a solution to this clinical problem without the need for oocyte donation program.

Read the detailed description

Premature ovarian insufficiency is a clinical syndrome characterized by early loss of ovarian function (less than 40 years of age) manifested by menstrual irregularity or amenorrhea with elevated levels of gonadotrophin hormones and low estrogen and anti-Mullerian hormone. The average age for menopause is 50-52 years in the developed world ,it is believed that about 1% for women less than 40 years of age and 0.1 in less than 30 years of age has premature ovarian insufficiency.

Etiology of POI may be genetic, chromosomal, or auto immune.in addition to cancer treatment and surgical causes.

Hormonal replacement therapy is recommended for POI patients to alleviate vasomotor symptoms in addition to prevent osteoporosis and ischemic heart disease.

Regenerative medicine is a new medical approach to treat variety of diseases involving many tissues or organs in human body using cells, biological products instead of drugs or physical factors.

Autologous use of stem cells from bone marrow or adipose tissue (stromal vascular fraction) or platelet rich plasma are alternative safe minimal manipulative products that can provide a solution to this clinical syndrome.

Only few cases had been mentioned in the literature offering autologous stem cells for treating POI including bone marrow or adipose derived stem cells in addition to mesenchymal stem cells expanded invitro.

the investigator use autologous bone marrow concentrate with transvaginal approach under ultrasound guidance to treat POI.

02

Conditions studied

  • Premature Ovarian Insufficiency

Keywords

  • premature ovarian failure,bone marrow,treatment
03

In context

Primary Ovarian Insufficiency

172 studies on the registry are indexed under Primary Ovarian Insufficiency; 45 are open to participants now.

This study's enrollment of 10 is below the median of 49 across 109 interventional studies indexed under Primary Ovarian Insufficiency.

Browse Primary Ovarian Insufficiency studies →

Lead sponsor

abdulmajeed hammadi is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
30 Years to 60 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  1. clinical diagnosis of premature Ovarian insufficiency.
  2. ineffective hormonal therapy.
  3. biochemical evidence of high gonadotropins.

Exclusion criteria

Exclusion criteria:

  1. solid or hematological malignancies.
  2. bleeding disorders.
  3. rejection of the procedure.
05

Study design

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

Study arms

  • Experimental
    bone marrow

    autologous bone marrow derived mononuclear cells injected 1cc per ovary for 2 ovaries under general anesthesia under ultrasound guide

    Procedure: autologous bone marrow cells injection

Interventions

  • Procedureautologous bone marrow cells injection

    under general anesthesia bone marrow aspiration done followed by cell concentration and transvaginal ovarian injection

06

What researchers measure

Primary outcomes

  1. change in gonadotropin levels

    luteinizing hormone and follicular stimulating hormone are followed

    Time frame: check every 4 weeks through study completion, an average of 1 year".

07

Study locations

1 site
  • Ministry of Health
    Baghdad, Iraq 964, Iraq
08

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 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06302543
Lead sponsor
abdulmajeed hammadi
Responsible party
abdulmajeed hammadi (clinical professor, Global Stem Cell Center, Baghdad) — Sponsor-investigator
First posted
Mar 8, 2024
Start date
Mar 1, 2024
Primary completion
Mar 10, 2026
Completion
Aug 10, 2026
Last update
Sep 14, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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