Health Condition 1: null- IUI & IVF Patients
Conditions
Interventions
None listed
Sponsors
Philips India Limited
Eligibility
Inclusion criteria
Inclusion criteria: • All subjects should be disease-free or presenting with one or more of the following history or complications: â?? Infertility (unknown etiology) â?? PCOS â?? Decreased ovarian reserve â?? Male infertility (female fertility check-up is normal) â?? Other causes of infertility â?? Ovarian cyst (endometrioma or other kind) â?? Other past or current history of medical disease unrelated directly to infertility provided the subject has the means to understand fully the information provided with the consent form â?? Current ovarian stimulation • The subjects enrolled should be either being screened for infertility or undergoing ovarian stimulation: spontaneous cycle, intra-uterine insemination, in vitro fecundation, in vitro-maturation, or other methods of ovarian ovulation stimulation.
Exclusion criteria
Exclusion criteria: • Subjects with neurological or psychiatric disorders or other disorders that affect the subjectâ??s understanding of the information provided with the consent form. • Breastfeeding subjects. • Subjects undergoing ovarian stimulation for surrogacy
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| To Find a potential scan protocol for follicular assessment that could help in developing more accurate algorithms. - Collect data of 2D US images and video of ovarian and uterine measurements (volumes) and endometrium thickness (ET) to build algorithms for automation of these assessments - Collect longitudinal data to track on 2D US, the growth of follicles in a given menstrual cycle Timepoint: 8 Months | — |
Primary
| Measure | Time frame |
|---|---|
| To collect videos and images of ovarian follicles using a 2D US device to build algorithms for semi-automation of follicle count and follicle measurements for women undergoing infertility work up or infertility treatment. We will compare the results of our algorithms with the benchmarked results provided by the sonologists. We will further evaluate the algorithms developed in this study by testing them in a later study using a different dataset (validation study).Timepoint: 8 Months | — |
Countries
India
Contacts
Public ContactRamachandran Ganesan
Philips India Limited
Outcome results
None listed