Skip to content

Effect of Painless Delivery on Maternal and Infant Outcome of 406 Cases of Vaginal birth after cesarean: Multicenter, Large Sample, Prospective Cohort Study, Differential Clinical Trial

Effect of Painless Delivery on Maternal and Infant Outcome of 406 Cases of Vaginal birth after cesarean: Multicenter, Large Sample, Prospective Cohort Study, Differential Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17010654
Enrollment
Unknown
Registered
2017-02-16
Start date
2017-02-18
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Effect of Painless Delivery on Maternal and Infant Outcome of 406 Cases of Vaginal birth after cesarean

Interventions

study group:painless labor
control group:none

Sponsors

Shenzhen Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 45 Years

Inclusion criteria

Inclusion criteria: (ASA I, II) single gestation of the gestational age of 35 weeks of gestation of the uterus by the maternal, heart, lung, liver, kidney, endocrine and endometriosis of the uterus in the vaginal test production of the indications (by the obstetrician) Nervous system serious disease, there is no application of systemic analgesics.

Exclusion criteria

Exclusion criteria: (1) maternal risk factors: prenatal depression, morbid obesity, unsafe airway, high risk of childbirth, the current low back pain, hemp and other symptoms of nerve stimulation; (2) Absolute and relative contraindications to spinal anesthesia and analgesia: patient refusal, puncture site infection, coagulopathy, unresolved hypovolemia, increased intracranial pressure, severe cardiovascular stenosis, local anesthetic allergy, resuscitation Inadequate medication or first aid equipment is not available, the patient does not meet the previous neurological deficits, spinal deformity or previous history of spinal surgery, thrombocytopenia; (3) of the uterus vaginal test production contraindications.

Design outcomes

Secondary

MeasureTime frame
Postpartum hemorrhage hemorrhage;Postpartum uterine rupture;labor;Analgesic effect and exercise block;Apgar score;Umbilical artery blood gas;placental blood flow;Postpartum lower limb neurological dysfunction;Postpartum depression;Postpartum chronic pain;Postpartum discomfort;Adverse reactions during analgesia;Postpartum adverse reactions;

Primary

MeasureTime frame
Birth success rate;

Countries

China

Contacts

Public ContactJing Sun

Shenzhen Maternal and Child Health Hospital

187244758@qq.com+86 13501597110

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 1, 2026