artificial insemination. Complications associated with artificial fertilization
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Couples with male-caused infertility (oligospermia) (total sperm count less than 15 million/ml), women aged 20 to 37 years, male partners aged 20 to 40 years, patients in their first or second cycle of IVF treatment.
Exclusion criteria
Exclusion criteria: Exclusion criteria included men with normal sperm parameters, varicocele patients, OAT (oligoastheno-teratozoospermia) patients, female infertility, women over 37 years of age, fresh transfer candidate patients, and patients who did not wish to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The outcomes of artificial insemination using ICSI in men with oligospermia. Timepoint: 6 MONTH. Method of measurement: A prospective randomized controlled clinical trial study, a total of 84 couples will participate in the study, with 42 couples in each group. On the day of egg retrieval and intracytoplasmic sperm injection in the first group, a microfluidic chip will be used to separate sperm before ICSI. Briefly, in this method, 850 µl of semen will be poured into the chip inlet and 700 µl of sperm washing medium previously warmed to 37°C will be poured into the chip outlet (containing a microporous membrane). The sperm will pass through the microchannels and pores of the microporous membrane and enter the outlet. Then the chip will be incubated for half an hour in a 37°C incubator. Finally, we will collect sperm at about 650 µm from the chip outlet.In the second group (control), the traditional swim-up technique will be used to select sperm for ICSI. | — |
Secondary
| Measure | Time frame |
|---|---|
| No. Timepoint: No. Method of measurement: No. | — |
Countries
Iran (Islamic Republic of)
Contacts
Bandare-abbas University of Medical Sciences