Randomized clinical trial assessing the effect of intravenous fluid restriction on outcome after elective liver resection

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-09000557

Enrollment

Unknown

Registered

2009-09-09

Start date

2005-11-01

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

Benign and Malignant Hepatobiliary Diseases

Interventions

restricted group:receive intraoperative and postoperative intravenous fluid regimen aimed at maintaining preoperative body weight

conventional group:intraoperative and postoperative intravenous fluid regimen resembles everyday practice

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing elective liver resection were considered eligible for the study

Exclusion criteria

Exclusion criteria: Less than 18 years, pregnancy, lactation, anemia, mental disorders, language problems, diabetes mellitus, cardiac failure, renal insufficiency, disseminated cancer, secondary cancers, emergency situations, contraindication to epidural anesthesia, required biliary reconstruction, or diseases hindering epidural analgesia, coagulopathy, alcohol abuse.

Design outcomes

Primary

Measure	Time frame
complications;	—

Secondary

Measure	Time frame
first bowel movement and length of postoperative hospitalization;	—

Countries

China

Contacts

Public ContactDexin Lin

ldx566@126.com+86 13957762646

Outcome results

None listed

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