Intraoperative crystalloids management using stroke volume variation in high risk patients

Intraoperative crystalloids management using stroke volume variation in high risk patients: a randomized control study

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-13003890

Enrollment

Unknown

Registered

2013-11-06

Start date

2013-11-20

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Surgical disease

Interventions

SVV group:SVV monitoring

Regular monitoring:Regular monitoring

Eligibility

Sex/Gender

All

Age

65 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. age: elder than 65 years, ASA 3 or more for comobidity such as diabetes mellitus, kidney disease,pulmonary disease,cardiovascular disease and etc.; 2. Operation duration more than 2 hours or presumed blood loss more than 800ml.

Exclusion criteria

Exclusion criteria: 1. Arhythmia,intracardial shunt; 2. Intolerance of tidal volume 8ml/kg with mechanical ventilation; 3. Renal failure and need for dialysis; 4. Thoracotomy; 5. Laparoscopic surgery; 6. Refusal of consent.

Design outcomes

Primary

Measure	Time frame
ECG, ABP, CVP, SpO2, EtCO2, temporature, urine,;	—

Contacts

Public ContactDongxin Wang

First Hospital of Peking University

wangdongxin@hotmail.com+86 010-83575138

Outcome results

None listed

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