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Role of Sub- endometrial implantation of autologous stem cells in women with Ashermanâ??s Syndrome and poor endometrium â?? A Pilot study.

Role of Sub- endometrial implantation of autologous stem cells in women with Ashermanâ??s Syndrome and poor endometrium â?? A Pilot study.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/08/003896
Enrollment
20
Registered
2013-08-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Intrauterine adhesions,Oligomenorrhea,Infertility

Interventions

Intervention1: AUTOLOGOUS HAEMOPOIETIC STEM CELLS: BONE MARROW MONONUCLEAR CELL SEPARATION 1. Bone Marrow (BM) Aspiration: Bone marrow (average 40-50 ml) will be aspirated from iliac crest/sternum u
The harvested mononuclear cells will evaluated for: 1. Viability test: Trypan blue dye exclusion test will be done to know the percentage of live cells. 2. Cell morphology: MNC will be stained with
Intervention2: AUTOLOGOUS HAEMOPOIETIC STEM CELL: 1. Bone Marrow (BM) Aspiration: Bone marrow (average 40-50 ml) will be aspirated from iliac crest/sternum using disposable bone marrow aspiration nee

Sponsors

All India Institute of Medical Sciences AIIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1Women in reproductive age group with primary or secondary infertility due to severe Ashermans Syndrome, with menstrual irregularities. 2Hypomenorrhoea, oligomenorrhoea or amenorrhoea 3 In whom the available treatment options that is hysteroscopic adhesiolysis and followed by estrogen stimulation have failed. 4Women willing to participate in the study.

Exclusion criteria

Exclusion criteria: Women more than 40 years of age are not included in the study. ?Patients with active endometrial tuberculosis. ?Patients with chronic debilitating diseases and or hematopoietic diseases affecting the bone marrow. ?Women not willing to participate

Design outcomes

Primary

MeasureTime frame
1.Attaining menstruation 2.Gain in Endometrial Thickness 3.Conception Timepoint: NOT APPLICABLE

Secondary

MeasureTime frame
Not ApplicableTimepoint: Not Applicable

Countries

India

Contacts

Public ContactDR NEETA SINGH

AIIMS

deneetasingh@yahoo.com26594251

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026