IVF.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women candidates for IVF Patients with antimullerian hormone more than 0.7 Women between 18 and 40 years old
Exclusion criteria
Exclusion criteria: The patient's reluctance to participate in the study Patients with a poor ovarian response (in terms of number of antral follicles and antimullerian hormone) Obesity (BMI above 35) Uterus anatomical problems
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain severity. Timepoint: During the ultrasound, At the end of the ultrasound. Method of measurement: Number one as the least pain and number ten as the most pain. Measuring of the variable will be done using the Numeric Pain Rating Scale method. In this method, the person rates their pain using a scale of 0 to 10. Zero means painless and 10 means the worst pain situation.;Ultrasonic visualization of the doctor. Timepoint: At the end of the ultrasound. Method of measurement: Appropriate / inappropriate. This variable will be done by asking the doctor at the end of the ultrasound. In this way, the degree of difficulty and three-dimensional vision of the doctor using this method will be recorded based on the physician's opinion.;Processing time. Timepoint: At the end of the ultrasound. Method of measurement: Second. The duration of the ultrasound at the end of the work will be recorded using a stopwatch in according to seconds.;Successful pregnancy. Timepoint: It will be done 4 weeks after embryo transfer. Method of measurement: Yes/No. Successful pregnancy will be recorded using beta-HCG measurement.;Frequency of tenaculum. Timepoint: At the end of the ultrasound. Method of measurement: It was used or not. Using or not of tenaculum will be reported at the end of sonography. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shahid Beheshti University of Medical Sciences