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Randomized controlled trial for comparison of different vasopressors for management of post-spinal hypotension in twin pregnancy.

Randomized controlled trial for comparison of different vasopressors for management of post-spinal hypotension in twin pregnancy.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013358
Enrollment
Unknown
Registered
2017-11-13
Start date
2017-12-01
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

post-spinal hypotension

Interventions

PHE group:Phenylephrine
NE group:Norepinephrine

Sponsors

Shanghai First Maternity and Infant Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists physical status 1 to 2, twin pregnancy, at term (37–38 weeks) and scheduled for elective cesarean delivery under routine spinal anesthesia.

Exclusion criteria

Exclusion criteria: Exclusion criteria included pre-existing/pregnancy-induced hypertension, known cardiovascular/cerebrovascular diseases, known fetal abnormality, allergy to study medications, extreme weight (100 kg) or height (180 cm), or those with contraindications for spinal anesthesia.

Design outcomes

Primary

MeasureTime frame
cardiac output;—

Secondary

MeasureTime frame
Blood pressure;heart rate;systemic vascular resistance;Apgar scores;—

Countries

China

Contacts

Public ContactWeijia Du

Shanghai First Maternity and Infant Hospital

duweijia@51mch.com+86 13817253768

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026