From patient charts we will review patients who had undergone cesarean section within the last 6 months and identify those who received a The Hayman uterine compression suture for uterine atony. We will also select patients who delivered a baby without recieving a Hayman suture to create a control group. Patietns will be grouped as Hayman Group if they recevied a Hayman suture during C/S and control group if thay had not recevied a Hayman suture. We will then check patient charts for post-cesarean outpatient clinic visit and select those who received ovarian reserve evaluation via hormones and antral follicle count during the visits. Finally, we are planning to investigate any correlation between Hayman suture and ovarian dysfunction.
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Change in anti-mullerian hormone level from baseline (precesarean) to post-cesarean
Timeframe: Before cesarean section and at any follow-up visit within 6 months of cesarean section
Change in follicle stimulating hormone level from baseline (precesarean) to post-cesarean
Timeframe: Before cesarean section and at any follow-up visit within 6 months of cesarean section
Change in luteinizing hormone level from baseline (precesarean) to post-cesarean
Timeframe: Before cesarean section and at any follow-up visit within 6 months of cesarean section