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Correlation Between the Polymorphism ofβ2 AR and the Labor Progress After Labor Analgesia

Principal Investigator

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02708602
Enrollment
300
Registered
2016-03-15
Start date
2016-03-31
Completion date
2016-05-31
Last updated
2016-03-17

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

Conditions

Labor Analgesia

Keywords

β2-adrenergic receptor, genetic polymorphisms, labor progress

Brief summary

Labor and delivery is a unique physiological experience of women. Inappropriate length of labor progress during vaginal delivery may produce great risks for mother and fetus. Especially the slow progress is one of the most important reasons for the occurrence of cesarean section during vaginal delivery, which still with a high incidence in recent years.Previous studies have found that there was a significant correlation between the genetic polymorphisms of β 2-adrenergic receptor (β2AR) and the duration of vaginal delivery.Therefore, the researchers intend to investigate the distribution of β2-adrenergic receptor (β2AR) genetic polymorphisms among Chinese parturient and observe the relationship between the genetic polymorphisms and labor process after labor analgesia.

Interventions

GENETICβ2AR polymorphism

Sponsors

Nanjing Maternity and Child Health Care Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
23 Years to 43 Years
Healthy volunteers
No

Inclusion criteria

* Nulliparous women * Required labor analgesia * Chinese * Spontaneous labor

Exclusion criteria

* Contraindications for epidural analgesia * Allergic to opioids and/or local anesthetics * Failed to performing epidural catheterization * Organic dysfunction * Those who were not willing to or could not finish the whole study at any time * Using or used in the past 14 days of the monoamine oxidase inhibitors * Alcohol addictive or narcotic dependent patients * Subjects with a nonvertex presentation or scheduled induction of labor * Twin gestation and breech presentation

Design outcomes

Primary

MeasureTime frameDescription
total labor processup to about 24htime from the regular uterus contractions until completed childbirth, assessed up to about 24h
duration of the first stageup to about 20htime from the regular uterus contractions to full cervix dilation,assessed up to about 20h
duration of the second stageup to about 2htime from full cervix dilation to the complete childbirth, assessed up to about 2h
Maternal visual analogue scaleAt time of initiation of analgesia and hourly thereafter until 2 hours postpartum (approximately 10 hours)At time of initiation of analgesia and hourly thereafter until 2 hours postpartum (approximately 10 hours)

Secondary

MeasureTime frameDescription
Use of oxytocin after analgesiaAt twenty-four hours postpartumAt twenty-four hours postpartum
Neonatal Apgar scaleAt the first and fifth minutes after baby was bornAt the first and fifth minutes after baby was born
method of deliveryAt time of placental deliveryAt time of placental delivery
Maternal heart rate, respiratory rate, and blood pressureAt time of initiation of analgesia and hourly thereafter until 4 hours postpartum (approximately 12 hours)At time of initiation of analgesia and hourly thereafter until 4 hours postpartum (approximately 12 hours)
Neonatal weightAt deliveryAt delivery
Maximal oxytocin doseAt twenty-four hours postpartumAt twenty-four hours postpartum
Maternal modified Bromage scaleAt time of initiation of analgesia and hourly thereafter until 2 hours postpartum (approximately 10 hours)At time of initiation of analgesia and hourly thereafter until 2 hours postpartum (approximately 10 hours)
Rescue boluses, n of rescue boluses, and the consumption of the ropivacaine/sufentanil mixtureAt two hours postpartumAt two hours postpartum
Maternal satisfaction with analgesiaAt two hours postpartumAt two hours postpartum

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026