FindTrial
Sign In

Comparative study on tolerance of continuous and intermittent enteral nutrition to enteral nutrition in severe patients

Comparative study on tolerance of continuous and intermittent enteral nutrition to enteral nutrition in severe patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066063
Enrollment
Unknown
Registered
2022-11-23
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

patient in severe condition

Interventions

continuous feeding group:no
intermittent feeding group :N/A

Sponsors

Suzhou University attached first hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Age = 18 years; ? The patient started enteral nutrition within 48 hours after admission to the ICU ? The patient's hemodynamics was stable.

Exclusion criteria

Exclusion criteria: The patient has a history of prokinetic anaphylaxis, gastrointestinal bleeding, intestinal obstruction, refractory vomiting or diarrhea, epilepsy or pheochromocytoma, orthotopic enterostomy or gastrostomy, nasogastric tube insertion or maintenance difficulties, or the patient needs a special feeding program (such as hemodialysis, chronic renal failure or diabetic diet), has undergone abdominal surgery within one month, or is pregnant.

Design outcomes

Primary

MeasureTime frame
diarrhea;Gastric retention;Aspiration;—

Countries

China

Contacts

Public Contactchenyamei

Suzhou University attached first hospital

2906232405@qq.com15962536216

Outcome results

None listed

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