Skip to content

Clinical study of enteral nutrition add ShenLingBaiZhu powder effect on the prognosis of critically ill patients

Clinical study of enteral nutrition add ShenLingBaiZhu powder effect on the prognosis of critically ill patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010467
Enrollment
Unknown
Registered
2017-01-18
Start date
2017-02-01
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

Prognosis of critically ill patients

Interventions

Experience group:Shenlingbaizhu powder
control group:placebo

Sponsors

Affiliated Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Signed informed consent; ICU patients; aged 18-85 years; APACHE score than less than or equal to 25 but more than 15 points; to enteral nutrition and enteral nutrition time more than 72 hours of ICU patients.

Exclusion criteria

Exclusion criteria: Give up the treatment of drugs used in the scheme; allergy; been currently participating in the studies of other drugs; APACHE II score 25 points; there are contraindications to enteral nutrition; there is partial or complete intestinal obstruction, intestinal ischemia or infarction there; gastrointestinal syndrome or short bowel syndrome (small intestine length less than 22cm); the doctors prescribed, at the beginning of the study SHENLINGBAISHU treatment within 2 weeks before receiving the expected death within 48 hours; patients; at the same time to participate in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Length of stay;Ventilator use time;Routine blood test;liver function;

Countries

China

Contacts

Public ContactPeiyang Gao

Affiliated Hospital of Chengdu University of Traditional Chinese Medicine

gaopy930@126.com+86 18980025566

Outcome results

None listed

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