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Assess Intrapartum Pain Relief after Epidural Analgesia With Facial Expressions Information Using Artificial Neural Networks

Assess Intrapartum Pain Relief after Epidural Analgesia With Facial Expressions Information Using Artificial Neural Networks

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018753
Enrollment
Unknown
Registered
2018-10-08
Start date
2018-11-15
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Intrapartum Pain

Interventions

expressions&#32
(facial&#32
expression&#32
model)
model&#32
based&#32
on&#32
Gold Standard:standard self-reported pain scores
Index test:personalized&#32
deep&#32
learning&#32

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Age 18 to 40 years old; (2) ASA grade 1-2; (3) No contraindications related to epidural anesthesia; (4) Not combining other diseases that cause pain; (5) No mental illness or other diseases affecting cognitive function; (6) Vaginal delivery and epidural anesthesia for labor analgesia; (7) Maternal women volunteered to participate in the trial and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) The face has obvious burns, scar contractures or trauma affecting facial recognition; (2) Maternal epidural anesthesia contraindications: central system diseases (e.g. meningitis, tuberculosis and tumors), spinal deformity, puncture site infection, sepsis, cardiovascular insufficiency (e.g. severe anemia, shock, heart failure, crown Heart disease), coagulopathy (platelets below 80*109/L, PT exceeds normal value for 3 seconds, TT exceeds normal value for 5 seconds, APTT exceeds normal value for 10 seconds); (3) The maternal woman cannot perform epidural anesthesia with the pendulum position; (4) Currently participating in another study that may interfere with the results of this study; (5) Other circumstances that the investigator determines are not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;SPE, SEN, ACC, ROC;

Secondary

MeasureTime frame
Facial Expressions;Self-rating Anxiety Scale;Pain Catastrophizing Scale;Self-rating Depression Scale;

Countries

China

Contacts

Public ContactWei Zhang

The First Affiliated Hospital of Zhengzhou University, Henan, PR China

zhangw571012@126.com+86 13673996966

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026