Bone Marrow Derived Stem Cells Mobilization for Treatment of Abnormal Endometrium
Recruiting now · Early Phase 1
Conditions studied: Asherman Syndrome, Atrophic Endometrium, Recurrent Implantation Failure
In brief
This study will assess the use of autologous bone marrow stem cells mobilization using 1,1'-\[1,4-phenylenebis-(methylene)\]-bis-1,4,8,11-tetraazacyclotetradecane (PLERIXAFOR) as an effective medical therapy for the treatment of Asherman's Syndrome (AS), Atrophic Endometrium (AE) and Recurrent Implantation Failure (RIF).
Key facts
- Study ID
- NCT05343572
- Run by
- Hugh Taylor
- People needed
- 90
- Starts
- 2023-11-01
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2025-11-12
Who can join
Age: 18 and older, up to 40. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Healthy, non pregnant females
- ages ≥18 and ≤40 years old at time of enrollment
- with either AS, AE, or RIF
- For AS: surgical history of intrauterine trauma/infection, hypo/amenorrhea, intra-uterine adhesions
- for AE: US documentation of persistent, <6mm endometrial thickness
- for RIF: failure to achieve a clinical pregnancy after transfer of at least four good-quality embryos in a minimum of three fresh or frozen cycles in a woman under 40 years and currently being treated at Yale Fertility Clinic
You may not qualify if…
- Presence of hydrosalpinx (diagnosed by radiographic or ultrasound imaging)
- Endometriosis (diagnosed by previous surgery,)
- Diminished ovarian reserve (AMH<1ng/ml or follicle stimulating hormone (FSH)>10)
- History of genital tuberculosis or any ultrasound evidence of congenital uterine anomaly
- Submucous or intracavitary fibroid, polyps
- Currently pregnant
- Personal history of thrombophilia or sickle cell disease
- Inability to provide informed consent
Where it is running
- Yale Fertility Center — Orange, Connecticut, United States (enrolling)
Full record on ClinicalTrials.gov
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