The role of perioperative pulmonary ultrasound in predicting volume overload in high-risk cesarean section patients: an observational, single center, prospective study

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100048933

Enrollment

Unknown

Registered

2021-07-19

Start date

2021-07-18

Completion date

Unknown

Last updated

2022-03-28

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

Conditions

High risk pregnancy

Interventions

case series:none

Eligibility

Sex/Gender

Female

Age

18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Patients who have a caesarean section in the selection; 3. Patients with high-risk pregnancy (eduzen and seizure seizure, double tire and multi-pregnant, etc.); 4. ASA II-III.

Exclusion criteria

Exclusion criteria: 1. Combined with severe heart disease or lung disease (patients diagnosed as pulmonary edema, etc.); 2. General anesthesia caesarean section; 3. Spinal temporal anesthesia contraindication (spinal malformation, history of trauma, anesthetic drug allergy, etc.); 4. Severe incomplete liver and kidney function; 5. Refuse to participate in research.

Design outcomes

Primary

Measure	Time frame
The relationship between the ultrasonic abnormality of the lungs (each region >= 3 B lines) and BNP within 48 hours after cesarean section;	—

Countries

China

Contacts

Public ContactLuo Dong

Huaxi Second Hospital of Sichuan University

luodong8706@163.com+86 18180609221

Outcome results

None listed

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