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Effect of preventive phenylephrine on Transient Tachypnea of Newborns after elective cesarean section under spinal anesthesia: a randomized controlled trial.

Effect of preventive phenylephrine on Transient Tachypnea of Newborns after elective cesarean section under spinal anesthesia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032974
Enrollment
Unknown
Registered
2020-05-17
Start date
2020-05-18
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Transient Tachypnea of Newborns

Interventions

experimental group:prophylactic using of phenylephrine
Control group:not prophylactic using of phenylephrine

Sponsors

Obstetrics and Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Single-pregnancy pregnant women with 37 weeks and above of gestation, who intend to undergo elective caesarean section under spinal anesthesia for ASAI-II grade; (2) Weight between 50 and 100kg, height between 150 and 180cm.

Exclusion criteria

Exclusion criteria: (1) Hypertension during pregnancy or diabetes during pregnancy; (2) Maternal women have a history of asthma; (3) Maternal exposure to steroids;

Design outcomes

Primary

MeasureTime frame
the incidence of Transient Tachypnea of Newborns;

Secondary

MeasureTime frame
Incidence of maternal hypotension;Use of phenylephrine;

Countries

China

Contacts

Public ContactJiawei Chen

Obstetrics and Gynecology Hospital of Fudan University

cjw11172@163.com+86 021-63455050-8479

Outcome results

None listed

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