Intraoperative Fluid Management in Open Gastrointestinal Surgery: Goal Directed or Fluid Restriction?

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-12001991

Enrollment

Unknown

Registered

2012-03-05

Start date

2011-01-01

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

gastric or colonic cancer

Interventions

R-RL:a fixed administration of 4 mL/kg per hour of lactated Ringer's solution exclusively throughout the study.If urine output 11%

GD-C:received a fixed administration of 4 mL/kg per hour of lactated Ringer’s solution throughout the study. In addition, this group received 250 mL 6% hydroxyethyl starch (HES, 130/0.4) as a bolus in

Eligibility

Sex/Gender

All

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: patients with gastric or colonic cancer and aged 18-64 years old

Exclusion criteria

Exclusion criteria: patients with BMI>30, significant arrhythmias, cardiopulmonary dysfunction, extensive peripheral arterial occlusive disease, significant renal or liver diseases, pregnancy or lactation and coagulopathy

Design outcomes

Primary

Measure	Time frame
length of hospital stay;	—

Secondary

Measure	Time frame
postoperative complications;Flatus time;	—

Countries

China

Contacts

Public ContactJun Zhang

snapzhang@yahoo.com.cn+86 13817153025

Outcome results

None listed

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