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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05558046
Other study ID # 07/2022
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date October 1, 2022
Est. completion date June 20, 2023

Study information

Verified date September 2022
Source Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Contact Erman Ciftci, MD
Phone +905074422414
Email ermanciftci1@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Deoxyribonucleic acid (DNA) damage of granulosa cells obtained during oocyte retrieval will be evaluated by flow cytometry with detection of Histone H2A.X and Phosphorylated Gamma H2A.X protein levels in patients with low ovarian reserve and unexplained infertile patients as a control group undergoing intracytoplasmic sperm injection (ICSI) treatment. Fertilization, embryo quality, transfer rate, implantation, clinical pregnancy will be recorded as well as demographic data. DNA damage of granulosa cells will be compared between two groups. The effect of DNA damage of granulosa cells on fertilization, quality of oocyte and embryo, implantation, and clinical pregnancy will be also evaluated.


Description:

Granulosa cells surrounding the oocytes will be mechanically obtained during the oocyte pick-up procedure in women undergoing intracytoplasmic sperm injection (ICSI) treatment due to unexplained infertility and low ovarian reserve. Deoxyribonucleic acid (DNA) damage in these cells will be evaluated by flow cytometry. Fertilization rates, embryo quality by grading, and transfer rates will also be assessed. Implantation and clinical pregnancy rates will be recorded as well as demographic data such as age, body-mass index, smoking, alcohol use, employment, coexisting chronic disease, infertility duration, etiology of infertility, treatment protocol. Implantation will be evaluated by determination of serum human chorionic gonadotropin (hCG) at day 15 following an embryo transfer. Clinical pregnancy will be diagnosed upon presence of gestational sac on ultrasound examination. DNA damage of granulosa cells will be compared between low ovarian reserve group and control group. The effect of DNA damage of granulosa cells on fertilization, quality of oocyte and embryo, implantation, and clinical pregnancy will be also evaluated.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date June 20, 2023
Est. primary completion date March 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - For patients who are undergoing in Vitro Fertilization (IVF) treatment with Low ovarian reserve, Antimullerian Hormone level must be lower than 1 ng/mL - For patients who are undergoing in Vitro Fertilization (IVF) treatment with Unexplained infetility, Antimullerian Hormone level must be greater than 1,5 ng/mL Exclusion Criteria: - Chronic systemic disease (rheumatoid arthritis, hypertension, diabetes..) - Endocrinopathy (Thyroid, prolactin... abnormalities) - Chemotherapy or radiotherapy history - Endometriosis - Policystic ovary syndrome - Male infetility

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Zeynep Kamil Maternity and Pediatric Research and Training Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Determining the correlation of ovarian reserve and age factor with DNA Damage markers in granulosa cells. Demographic data will be noted for each patient at the day of oocyte retrieval, and DNA damage markers will be shown by flowcytometry at the same day. 1 day
Secondary Fertilization defined as the presence of two pronuclei under light microscope one day after intracytoplasmic sperm injection procedure Presence of two pronuclei under light microscope 1 day after ICSI procedure
Secondary Implantation defined as positive serum human chorionic gonadotropin levels 12 days after embryo transfer Positive human chorionic gonadotropin levels 12 days after embryo transfer
Secondary Clinical pregnancy will be defined as the presence of gestational sac in transvaginal ultrasonographic examination 5 weeks after embryo transfer Presence of a gestational sac in transvaginal ultrasonographic examination 5 weeks
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