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Study on the Effect of Capacity Shock Intervention Under Goal-directed Hemodynamic Management on P-V Loop

G

Guangzhou Red Cross Hospital

Status

Completed

Conditions

Hemodynamics

Treatments

Procedure: Fluid challenge strategy
Procedure: conventional strategy

Study type

Interventional

Funder types

Other

Identifiers

NCT04934761
202103000022

Details and patient eligibility

About

By observing the changes of P-V loop in capacity shock intervention Under Goal-directed Hemodynamic Management in patients undergoing total knee replacement, we investigate the effect of capacity shock on cardiac contractility and work in order to seek a more effective target plan of capacity shock for intraoperative patients.

Full description

Objective:By observing the changes of P-V loop in capacity shock intervention Under Goal-directed Hemodynamic Management in patients undergoing total knee replacement, we investigate the effect of capacity shock on cardiac contractility and work in order to seek a more effective target plan of capacity shock for intraoperative patients.

Methods:20 patients with total knee replacement were enrolled in this study. Capacity shock therapy was used in Group A(n=10) and conventional strategy was used in Group B (n=10). V(t) was measured and calculated using TEE and P(t) was acquired by the analysis of patients'radial artery pressure waveform. We set five time points of parameter acquisition: after grouping (T1), the first shock completion(T2), the second shock completion (T3), 1h after shock treatment (T4), and operation completion(T5). We make up the P-V loop fitting P(t) and V(t) at each time point after the calibration of cardiac cycle.

Enrollment

20 patients

Sex

All

Ages

40 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

ASAI-II age 40- 70 weight 48 - 72 kg.

Exclusion criteria

Body mass index >30 or <15 kg/m2 Valve heart disease Left ventricular ejection fraction (LVEF) is less than 50% History of lung disease Preoperative arrhythmic disorder Permanent pacemaker Need for mechanical heart Support, Severe extrinsic vascular disease Valve dysfunction OED monitoring probe insertion contraindications Patients with preoperative assessments

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

20 participants in 2 patient groups

capacity shock
Experimental group
Description:
2ml/kg succinylateol gelatin
Treatment:
Procedure: Fluid challenge strategy
routine management
Other group
Description:
conventional strategy
Treatment:
Procedure: conventional strategy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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