Parameter | Inclusion criteria | Exclusion criteria |
---|---|---|
P articipants | • Couples 18 years of age and older with infertility |  |
I nterventions | • IVF/ICSI | • GIFT/ZIFT |
 | • In vitro maturation | |
C omparators | • Spontaneous/natural conception | Studies comparing different drugs or drug regimens used |
• Less invasive ARTs (ovulation induction, intrauterine insemination) | • Studies assessing pre-treatment characteristics, such as embryo and uterine preparation techniques or hysteroscopy, or treatment ‘add-ons’, such as preimplantation genetic screening (PGS) or assisted hatching (AH) | |
• Procedural differences, including: |  | |
- the number of embryo’s transferred |  | |
- blastocyst vs. cleavage embryo transfers | Â | |
- frozen vs. fresh embryo transfers | Â | |
- autologous vs. donor embryo transfers | Â | |
O utcomes | Safety: | • Studies without any defined clinical outcomes |
• Neonatal/infant complications (e.g., ectopic pregnancy, low birth weight, neonatal/perinatal mortality, birth defects, congenital malformations) |  | |
• Pregnancy and delivery complications (e.g., OHSS, ectopic pregnancy, preeclampsia, caesarean delivery, preterm birth) |  | |
Effectiveness: | Â | |
• Indicators of cycle success (e.g., number of oocytes retrieved, cycle cancellation, implantation) |  | |
• Pregnancy, miscarriage, live birth |  | |
• Multiple pregnancy/multiple birth |  | |
S tudy design | • Systematic reviews | Primary studies* |