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Maternal and neonatal effects of sufentanil with different dosage during analgesia labor

Maternal and neonatal effects of sufentanil with different dosage during analgesia labor

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017833
Enrollment
Unknown
Registered
2018-08-16
Start date
2018-08-20
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

analgesia labor

Interventions

Group 2:sulfentanil0.5
Group 1:sulfentanil 0.25 mg

Sponsors

Department of Anesthesiology, International Peace Maternity and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. ASA Physical Status grade III, and a full term singleton, cephalic presentation and without prior use of opioid analgesics will be recruited; 2. Patients had regular prenatal examinations at the outpatient clinic; 3. Aged 25 to 35 years; 4. They had a gestational age 37 to 42 weeks; 5. They had an estimated fetal weight between 2,500 g to 4,200 g.

Exclusion criteria

Exclusion criteria: 1. Patients with any diagnosed cardiac diseases (e.g. cardiac failure, angina, MI, cardiac arrhythmia. etc.); 2. Patients with any diagnosed pulmonary disease (e.g. asthma, pulmonary embolism, pulmonary edema etc.); 3. Patients with coagulation disorder; 4. Patients with liver failure; 5. Patients with kidney failure; 6. Patient with a history of spinal surgery; 7. Patients with sensorimotor disorder of lower extremity; 8. Patients with SPO2 < 95% on room air; 9. Patient with a history of neuropsychopathy drugs.

Design outcomes

Primary

MeasureTime frame
VAS;

Countries

China

Contacts

Public ContactZeyong Yang

International Peace Maternity and Child Health Hospital

zeyongy2018@aliyun.com+86 021-64070434

Outcome results

None listed

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