Effect of Crystalloid and Colloid fluid Infusion on patients undergoing abdominal surgery with Da Vinci robot under Target guided fluid Therapy

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900024397

Enrollment

Unknown

Registered

2019-07-10

Start date

2019-07-16

Completion date

Unknown

Last updated

2019-07-15

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

Conditions

Colorectal cancer and gynecological malignant tumor

Interventions

1:crystalloid therapy

2:colloid therapy

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1 Elective radical resection of colorectal cancer and gynecological malignant tumor by da Vinci robot; 2 ASA grade I ~ II; 3 Aged > 18 years; 4 BMI 18.5 to 25 kg/m2.

Exclusion criteria

Exclusion criteria: 1 Preoperative infection; 2 Severe arrhythmias / atrial fibrillation; 3 Colloid allergies; 4 Patients with severe cardiopulmonary, hepatic and renal dysfunction; 5 The amount of blood lost during operation was more than that of 1000ml; 6 Those who refuse to sign informed consent; 7 Emergency surgery; 8 The operation time is less than 2 hours.

Design outcomes

Primary

Measure	Time frame
Recovery time of gastrointestinal function after operation;	—

Secondary

Measure	Time frame
Postoperative Morbidity Survey , POMS;acute kidney injury,AKI;	—

Countries

China

Contacts

Public ContactWang Lulu

The First Affiliated Hospital of Zhengzhou University

990691695@qq.com+86 15138473481

Outcome results

None listed

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