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Hemodynamic Management in Women With SHS

C

China Medical University, China

Status

Enrolling

Conditions

Supine Hypotensive Syndrome

Treatments

Procedure: LiDCOrapid

Study type

Interventional

Funder types

Other

Identifiers

NCT05341362
SHSandLidco

Details and patient eligibility

About

Supine hypotensive syndrome often occurs following spinal anesthesia for cesarean delivery.In our study we base the regulation and drug administration both on the regular monitor and on a novel monitor which reflects upon the hemodynamic changes. Our aim is to observe whether the outcome of SHS patients with anesthesia management based on hemodynamic figures differs from those based on experience.

Enrollment

60 estimated patients

Sex

Female

Ages

22 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • American Society of Anesthesiologists (ASA) Physical Status Classification II and had no significant cardiovascular, pulmonary, renal or endocrine disease, without contraindications to CSEA,and could be diagnosed as SHS according to the criteria.

Exclusion criteria

  • Patients undergoing emergency CD, CD under general anesthesia or patients' refusal to participate, or multiple fetations.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Blank Group
No Intervention group
Description:
In this group, the anesthesia management is conducted according to the anesthetists' experience, based on the regular monitor.
LiDCOrapid Group
Experimental group
Description:
In this group, the anesthesia management is conducted based on both the regular monitor and the hemodynamic figures on the LiDCOrapid.
Treatment:
Procedure: LiDCOrapid

Trial contacts and locations

1

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Central trial contact

Li Yuqing

Data sourced from clinicaltrials.gov

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