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To explore the effect of left tilt position on fetal heart rate in the early stage of labor analgesia

To explore the effect of left tilt position on fetal heart rate in the early stage of labor analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112899
Enrollment
Unknown
Registered
2025-11-20
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Abnormal fetal heart rate monitoring

Interventions

Left tilt position group:Left tilt position

Sponsors

Hangzhou Women's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Term singleton pregnancy with planned vaginal delivery; 2.Height: 150-180 cm; 3.ASA Grade II; 4.Body mass index (BMI) <35 kg·m^-2; 5.Fetal heart rate monitoring is classified as type I according to the NICHD guidelines; 6.Intraspinal labor analgesia is required

Exclusion criteria

Exclusion criteria: 1.Fetal macrosomia without cephalic presentation; 2.Uterine abnormalities (such as large fibroids, bicornuate uterus); 3.Polyhydramnios; 4.Rupture of membranes and oligohydramnios; 5.Intrauterine growth restriction; 6.Hypertension, diabetes or eclampsia during pregnancy or non-pregnancy; 7.Hypertension disease or any disorder related to autonomic neuropathy; 8.Contraindications for epidural anesthesia; 9.Subjects who refused to sign the informed consent form

Design outcomes

Primary

MeasureTime frame
Rate of NICHD guideline Type II or III patterns within 40 minutes after intrathecal labor analgesia;

Secondary

MeasureTime frame
Rate of NICHD guideline Type II patterns during 0–20 minutes and 20–40 minutes after intrathecal labor analgesia;Rate of NICHD guideline Type ? patterns during 0–20 minutes and 20–40 minutes after intrathecal labor analgesia;Fetal heart rate baseline, fetal heart rate accelerations, fetal heart rate decelerations, and fetal heart rate variability within 40 minutes after intrathecal labor analgesia;Neonatal outcomes: Apgar scores at 1 minute and 5 minutes after birth;Maternal analgesic efficacy evaluation: At immediate, 10 minutes, 20 minutes, 30 minutes, and 40 minutes after epidural loading dose administration, record pain score, sensory block level to temperature, motor block score, and number of patient-controlled analgesia bolus presses.;Maternal hemodynamic evaluation: Incidence of maternal hypotension, types and doses of vasopressor agents used.;Uterine contraction evaluation: Use of uterotonic agents and their dosages; uterine contraction patterns during the 40 minutes before and after labor analgesia (number of episodes and number of parturients experiencing uterine tachysystole and uterine hypertonus).;Mode of delivery: Number of vaginal deliveries, instrument-assisted deliveries, and conversions to cesarean section.;

Countries

China

Contacts

Public ContactZhou Zhenfeng

Hangzhou Women's Hospital

86833554@qq.com+86 571 56005000

Outcome results

None listed

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