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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05379582
Other study ID # 2022-050-02
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2022
Est. completion date June 1, 2023

Study information

Verified date April 2022
Source Chinese Medical Association
Contact Tao Gao, no
Phone +86-025-83106666
Email ggttt001@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In critical ill patients, feeding protocol is one of the important factor which determines the successful implementation of enteral nutrition(EN). Acute gastrointestinal injury(AGI) affects feeding tolerance, which greatly determines the successful implementation of feeding protocol. In our previously study, we found that transabdominal intestinal sonography is helpful to diagnosis AGI. Thus in this study ,we apply transabdominal gastrointestinal sonography to feeding protocol, to assess the feasibility of gastrointestinal sonography assisted enteral nutrition and its impact on critical ill patients.


Description:

Patients meeting inclusion and exclusion criteria were randomly assigned to the intervention group and control group. During the first week of initiation of nutrition, enteral nutrition was conducted according to different procedures to observe the impact of different feeding procedures on clinical indicators


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date June 1, 2023
Est. primary completion date April 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - The age is not less than 18 years - within 24 hours after entering ICU - Acute Physiology and Chronic Health Evaluation II (APACHE II) score > 8 - the estimated length of stay in ICU is more than 3 days - informed consent Exclusion Criteria: - The normal anatomy of stomach, small intestine or the right colon was significantly changed (Gastrectomy, esophagectomy, pancreaticoduodenectomy, gastrointestinal bypass surgery, the presence of short bowel syndrome,etc.) - Uncontrolled gastrointestinal bleeding - Uncontrolled intestinal obstruction - Uncontrolled mesenteric vascular disease - Pregnancy - breastfeeding - Received enteral nutrition or parenteral nutrition within 24 hours prior to ICU admission - Predict death within 48 hours after ICU admission - Enrolled in this study before.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Implement nutrition therapy according a procedure assisted by gastrointestinal ultrasound
Once the critical ill patients is stable, enteral nutrition was initiated following a procedure assisted by gastrointestinal ultrasound.

Locations

Country Name City State
China Nanjing Drum Tower Hospital Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Chinese Medical Association

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary mortality Day28 after enrollment
Primary mortality Day60 after enrollment
Primary mortality Day90 after enrollment
Primary Enteral nutrition support days within first seven days after enteral nutrition initiation
Primary Target-reaching rate through enteral route percentage of participants who reach target calorie through enteral route within first seven days after enteral nutrition initiation
Primary The application rate of parenteral nutrition(PN) percentage of participants who needs parenteral nutrition within first seven days after enteral nutrition initiation
Primary The application rate of prokinetic drugs percentage of participants who needs prokinetic drugs within first seven days after enteral nutrition initiation
Secondary Sequential Organ Failure Assessment score The value ranges from 0 to 24. A higher score means a worse outcome. The first day after enrollment.
Secondary Acute Physiology and Chronic Health Evaluation score The value ranges from 0 to 71. A higher score means a worse outcome. The first day after enrollment
Secondary The average dose of vasoactive drugs First week of the study
Secondary Days of vasoactive drugs Through study completion, an average of 1 year
Secondary Days of mechanical ventilation Through study completion, an average of 1 year
Secondary Days of continuous renal replacement Through study completion, an average of 1 year
Secondary Serum prealbumin in milligram/liter Day7 after enteral nutrition initiation
Secondary Serum prealbumin in milligram/liter Day14 after enteral nutrition initiation
Secondary Serum transferrin in milligram/liter Day7 after enteral nutrition initiation
Secondary Serum transferrin in milligram/liter Day14 after enteral nutrition initiation
Secondary The thickness of diaphragm under ultrasonography in centimeter Day7 after enteral nutrition initiation
Secondary The thickness of diaphragm under ultrasonography in centimeter Day14 after enteral nutrition initiation
Secondary The thickness of diaphragm under ultrasonography in centimeter Day28 after enteral nutrition initiation
Secondary The thickness of quadriceps under ultrasonography in centimeter Day7 after enteral nutrition initiation
Secondary The thickness of quadriceps under ultrasonography in centimeter Day14 after enteral nutrition initiation
Secondary The thickness of quadriceps under ultrasonography in centimeter Day28 after enteral nutrition initiation
Secondary The strength of upper limb according to the Lovett muscle strength scale The value ranges from 0 to 5. A higher score means a better outcome. Day7 after enteral nutrition initiation
Secondary The strength of upper limb according to the Lovett muscle strength scale The value ranges from 0 to 5. A higher score means a better outcome. Day14 after enteral nutrition initiation
Secondary The strength of upper limb according to the Lovett muscle strength scale The value ranges from 0 to 5. A higher score means a better outcome. Day28 after enteral nutrition initiation
Secondary The strength of upper limb according to the Lovett muscle strength scale The value ranges from 0 to 5. A higher score means a better outcome. Through study completion, an average of 1 year.
Secondary The mid-arm circumference in centimeter Day7 after enteral nutrition initiation
Secondary The mid-arm circumference in centimeter Day14 after enteral nutrition initiation
Secondary The mid-arm circumference in centimeter Day28 after enteral nutrition initiation
Secondary The mid-arm circumference in centimeter Through study completion, an average of 1 year.
Secondary The Medical Research Council sum score The value ranges from 0 to 60. A higher score means a better outcome. Day14 after enteral nutrition initiation
Secondary The Medical Research Council sum score The value ranges from 0 to 60. A higher score means a better outcome. Day28 after enteral nutrition initiation
Secondary The Medical Research Council sum score The value ranges from 0 to 60. A higher score means a better outcome. Through study completion, an average of 1 year
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