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For Increase in Endometrial Thickness in Women With Thin Endometrium undergoing Infertility Treatment use of Intrauterine Infusion Of Autologous Platelet Rich Plasma (PRP) and Granulocyte Colony Stimulating Factor (G-CSF)

Intrauterine infusion of autologous platelet rich plasma (PRP) versus granulocyte colony stimulating factor (G-CSF) for thin endometrium in infertile women.

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064601
Enrollment
40
Registered
2024-03-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium

Interventions

Intervention1: Autologous platelet rich plasma: Intrauterine infusion of 1 ml of autologous platelet rich plasma will be performed with intrauterine insemination catheter under USG guidance. Endometri

Sponsors

Datta megha institute of higher education and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: women aged 18 to 45 years, thin endometrium less than 7 mm on the day of HCG injection, no contraindications for Platelet rich plasma (PRP) and Granulocyte colony stimulating factor(G-CSF) treatment, Women with a normal transvaginal ultrasound and no evidence of a clinically significant abnormality in the uterus or adnexa, Negative CBNAAT, negative AFB staining & negative TBPCR for genital tuberculosis.

Exclusion criteria

Exclusion criteria: patients with a body mass index more than 30 kg/m2, Positive history of intrauterine synechiae, repeated curettage, endometrial injury, Distorted endometrium cavity, submucosal fibroids, endometrial polyps, severe endometriosis, adenomyosis, pelvic cancer and uterine anomalies, chromosomal abnormalities in couples, patients with abnormal liver and kidney function, abnormal thyroid function, immune disorders, hematological disorders;

Design outcomes

Primary

MeasureTime frame
expansion of endometrial thickness (EMT)Timepoint: AT BASELINE, AFTER 10 DAYS, AFTER 12 DAYS, AFTER 14 DAYS , AFTER 16 DAYS

Secondary

MeasureTime frame
positive beta-hCG level ? implantation rate (IR), ? positive urine pregnancy test ? clinical pregnancy rate (CPR) by confirmation of Gestational sac with cardiac activity in Trans-vaginal sonography (TVS) ? live birth rate (LBR) (if possible within study periodTimepoint: 2 year

Countries

India

Contacts

Public ContactDr. Smruti Mapari

Datta Meghe Institute Of Higher Education and Research

deepti_shrivastava69@yahoo.com9860817801

Outcome results

None listed

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