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The research of bedside ultrasound in evaluating gastric motility of different infusion methods

The research of bedside ultrasound in evaluating gastric motility of different infusion methods

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018532
Enrollment
Unknown
Registered
2018-09-22
Start date
2018-10-08
Completion date
Unknown
Last updated
2018-10-01

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

Conditions

Respiratory disease

Interventions

Group A:Use nutrition pump to input continuously in the daytime,the infusion rate increased gradually from 30ml/h to 60ml/h.The infusion was completed within 10-12h. The infusion rate was decreased wh
Group B:In normal physiological feeding time, interval 4h to 6h takes three periods
7:00~9:00
1200-14:00
17:00~19:00, Use nutrient pump to discontinue nutrient solution. The infusion rate was 30 ml/h to 60 ml/h on the first day, 90 ml/h to 120 ml/h on the second day,If there is no abnormality, Adjust to

Sponsors

Huzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. conforming to the diagnostic criteria of chronic obstructive pulmonary disease (COPD) and type II respiratory failure; 2. having indications for non-invasive mechanical ventilation and estimated that the duration of non-invasive mechanical ventilation is longer than 3 days; 3. inability to swallow food orally or oral intake less than 50% of daily required nutrition; 4. Clear mind, be able to cooperate with communication and treatment; 5. Agde greater than or equal to 18 years old.

Exclusion criteria

Exclusion criteria: 1. ultrasonographic examination revealed abnormal organ morphology in digestive system; 2. having fstula, necrosis, obstruction, and surgery of gastrointestinal system; 3. Other serious medical conditions such as heart, liver and kidney dysfunction, cerebrovascular accident and ketoacidosis; 4. patients with unstable hemodynamics; 5. taking gastric motility drugs during the trial period; 6. BMI=30kg/m2; 7. need for changing diet or prescribing a specifc diet during the study; 8. pregnant woman.

Design outcomes

Primary

MeasureTime frame
Single section area of antrum;Gastrointestinal tolerance;

Secondary

MeasureTime frame
motilin;Melanin;

Countries

China

Contacts

Public ContactHua Feng

Huzhou Central Hospital

fan9010@msn.com+86 13587252299

Outcome results

None listed

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