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Common carotid artery corrected flow time to guide the prevention of maternal hypotension after spinal anesthesia: a prospective, double-blind, controlled study

Common carotid artery corrected flow time to guide the prevention of maternal hypotension after spinal anesthesia: a prospective, double-blind, controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084392
Enrollment
Unknown
Registered
2024-05-15
Start date
2024-05-20
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

None

Interventions

Nonvolemic response rehydration group:Within 20min before surgery, 500ml of hydroxyethyl starch 130/0.4 sodium chloride injection and 50ml of normal saline were continuously pumped at 0.05µg/kg/min un
Nonvolemic response norepinephrine group:The loading volume of norepinephrine 4 µg + 0.05 µg/kg/min was intravenously pushed 20 minutes before operation, and the pump was continued until the fetus was
A volume response rehydration group:Within 20min before surgery, 500ml of hydroxyethyl starch 130/0.4 sodium chloride injection and 50ml of normal saline were continuously pumped at 0.05µg/kg/min unti
A volume response to norepinephrine group:The loading volume of norepinephrine 4 µg + 0.05 µg/kg/min was intravenously pushed 20 minutes before operation, and the pump was continued until the fetus wa

Sponsors

Department of Anesthesiology, The first affiliated Wannan Medical College(Yijishan Hospital of Wannan Medical college)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 48 Years

Inclusion criteria

Inclusion criteria: ASAI-II, regular prenatal visits, age = 18 years, singleton pregnancy, = 37 weeks' gestation

Exclusion criteria

Exclusion criteria: Gestational hypertension, preeclampsia or emergency cesarean section or 50% history of common carotid artery stenosis, cardiovascular and cerebrovascular diseases, hypertension, chronic obstructive pulmonary disease, arrhythmia, diabetes, cerebrovascular disease, alcoholism, or pregnant women with psychiatric disorders, as well as severe vision, hearing or intellectual disabilities, speech disorders, unable to communicate or unwilling to participate in the study.

Design outcomes

Primary

MeasureTime frame
Incidence of hypotension;

Secondary

MeasureTime frame
Hemodynamic indicators;Intraoperative adverse events occurred;Umbilical cord blood gas index;Postoperative adverse events occurred;Neonatal Apgar score (1 min and 5 min);Duration of postoperative ventilation;Time to get out of bed after surgery;

Countries

China

Contacts

Public ContactChen Yongquan

Department of Anesthesiology, The first affiliated Wannan Medical College(Yijishan Hospital of Wannan Medical college)

2954821651@qq.com+86 139 5619 6920

Outcome results

None listed

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