A study on maternal stress and fetal stress during delivery.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000015745

Enrollment

Registered

2014-12-15

Start date

2014-12-15

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delivery

Interventions

It measures the blood glucose level, lactic acid value and the hematocrit value in the umbilical cord blood. Sampling the umbilical cord blood and maternal the maternal saliva (delivery before?deliver

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Pregnant women before, during and after delivery.

Exclusion criteria

Exclusion criteria: Cesarean section

Design outcomes

Primary

Measure	Time frame
The degree of variable deceleration detected by the delivery monitoring device.	—

Secondary

Measure	Time frame
Maternal stress marker(saliva cortisol concentration)and intrapartum umbilical cord blood stress markers (blood sugar) (lactic acid) (cortisol concentration) (oxytocin concentration).	—

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026