Health Condition 1: N972- Female infertility of uterine origin
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Women with Ashermanâ??s syndrome that have undergone hysteroscopic adhesiolysis resulting in Normal/optimal cavity size yet atrophic endometrium ( 2. Women with refractory atrophic endometrium ( 3. Willing to participate in the study
Exclusion criteria
Exclusion criteria: 1. Women with Ashermanâ??s syndrome after surgical correction with suboptimal uterine cavity 2. Genital tuberculosis (the disease has profound effects on compromising cavity size, compromising sub-endometrial vascularity and being a pilot work will be selective on cases) 3. Hematologic disorders, hemoglobin level of 4. Chronic autoimmune diseases 5. Refusal to participate in study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| This study will help in understanding the best strategy to regenerate endometrial lining in patients with refractory Ashermanâ??s syndrome and atrophic endometrium. By having a correlation of percentage of mononuclear and mesenchymal stem cells with the endometrial regeneration will be valuable in planning future studies. The analysis of growth factors in PRP and their effect on endometrial thickness will be of utmost importance for standardization of PRPTimepoint: All the patients will receive standard hormone replacement therapy and followed up at 1 month, 2 months, 3 months and 6 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| â?¢Standardization of PRP preparation â?¢This will open the pathway to future studies with larger sample size â?¢After we have the results and have an idea of best strategy to deal with refractory AS and atrophic endometrium, we can have further studies to evaluate role of PRP and stem cells in IVF cycles and compare with reproductive outcomes.Timepoint: 3 Years | — |
Countries
India
Contacts
AIIMS