Infertility Clinical Trial
— G-CSFOfficial title:
Intrauterine G-CSF Administration in Recurrent Implantation Failure
Verified date | December 2018 |
Source | Gurgan Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Aim of this study is to investigate the effects of intrauterine G-CSF on endometrial thickness, clinical pregnancy rate and live birth rate in a recurrent implantation failure (RIF) group
Status | Completed |
Enrollment | 157 |
Est. completion date | December 20, 2018 |
Est. primary completion date | December 20, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Women under the age of 40 who met the RIF definition - Follicle-stimulating hormone (FSH) levels were <15 IU/mL Exclusion Criteria: - Patients with congenital uterine anomalies - Patients with Asherman's syndrome - Patients with uterine cavity distorted by myoma or endometrial polyps - Patients with confirmed endometriosis or endometrioma - Patients for whom G-CSF was contraindicated (active infections, kidney disease, sickle cell anemia, malignancies, chronic neutropenia) |
Country | Name | City | State |
---|---|---|---|
Turkey | Gurgan Clinic IVF and Women Health Center | Ankara | Cankaya |
Lead Sponsor | Collaborator |
---|---|
Gurgan Clinic |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Clinical pregnancy rate | Gestational sac in USG per embryo transfer | 1month | |
Secondary | Endometrial thickness | Measurement of endometrial thickness as millimeter | 1month |
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