The Effects of Different Gastric Residual Volume Thresholds for Holding Feeding in Internal Medicine.

Critical Illness Clinical Trial

Official title:

Comparison of the Effects of Different Gastric Residual Volume Thresholds for Holding Enteral Feeding on Nutritional Intake in Critically Ill Patients in Internal Medicine

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06113393
• Other study ID #: 202307181RINB
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 2024
• Est. completion date: December 2024

Study information

• Verified date: October 2023
• Source: National Taiwan University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a randomized control trial with a parallel design. Eligible patients will be randomly assigned into two groups: a control group which will be holding tube feeding when the GRV reaches 200 mL, and an experimental group will hold tube feeding when the GRV reaches 300 mL. Enteral feeding will be administered according to the study flow chart.

Description:

Background: Malnutrition is a common issue among critically ill patients. which increases hospital stays, costs, and mortality rate. According to the study, the primary reason for nurses to hold enteral nutrition is elevated gastric residual volume (GRV). However, there is still no consensus on the definition of high residual gastric volume, there is currently no consensus among experts and scholars regarding the threshold for holding enteral nutrition. Clinical nurses may prematurely hold enteral nutrition due to concerns regarding potential side effects such as vomiting and choking. The aim of this study is to increase the threshold for holding enteral feeding based on the results of the study, in order to improve nutritional intake in critically ill patients in internal medicine. Objective: Increase the nutritional intake of critically ill patients in the Department of Internal Medicine by increasing the threshold for holding tube feeding. Methods: This is a randomized control trial with a parallel design. Eligible patients will be randomly assigned into two groups: a control group which will be holding tube feeding when the GRV reaches 200 mL, and an experimental group will hold tube feeding when the GRV reaches 300 mL. Enteral feeding will be administered according to the study flow chart. The outcome data will collected based on the medical chart including frequency of diet volume ratio (diet received/diet prescribed), incidence of gastrointestinal complications, ventilator days, Ventilator-associated pneumonia, length of intensive care unit(ICU) stay, changes in nutritional indicators, APACHE Ⅱ and Duration of parenteral nutrition use. Expected result: The results of this study will provide evidence regarding the improved effectiveness and safety of increasing the threshold of GRV in medical ICU and inform future evidence-based practice.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 230
• Est. completion date: December 2024
• Est. primary completion date: December 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult patients admitted to the internal medicine intensive care unit.
• Patients receive enteral nutrition through a nasogastric tube.
• Patients receiving continuous enteral feeding.

Exclusion Criteria:

• Patients post-abdominal surgery.
• Patients admitted to the intensive care unit due to gastrointestinal disorders (e.g., gastrointestinal bleeding, bowel obstruction).
• Patients receiving palliative care with reduced enteral nutrition.

Related Conditions & MeSH terms

• Critical Illness

Intervention

Procedure:
• GRV thresholds
Hold enteral feeding when GRV reaches 200 mL(current standard)

Locations

Country	Name	City	State
Taiwan	National Taiwan University Hospital	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of diet volume ratio		1 day (Transfer from the Intensive Care Unit)
Primary	Incidence of gastrointestinal complications	Abdominal distension, nausea, vomiting, diarrhea, constipation	1 day (Transfer from the Intensive Care Unit)
Secondary	Days of ventilator use		A week(Transfer from the Intensive Care Unit)
Secondary	Ventilator-associated pneumonia	Diagnosis form clinical doctor according to chest x-ray	1 day (Transfer from the Intensive Care Unit)
Secondary	Length of stay in the intensive care unit		A week(Transfer from the Intensive Care Unit)
Secondary	Days of parenteral nutrition use		A week(Transfer from the Intensive Care Unit)
Secondary	Acute Physiology and Chronic Health Evaluation score	an integer score from 0 to 71 is computed based on several measurements; higher scores correspond to more severe disease and a higher risk of death.	1 day (Transfer from the Intensive Care Unit)
Secondary	Nutrition Risk Screening 2002(NRS2002)	The NRS-2002 was developed by Kondrup et al., and is meant to be a generic tool in the hospital setting-that is, useful in detecting most of the patients who would benefit from nutritional therapy. The NRS-2002 is a simple and well-validated tool that incorporates pre-screening with four questions. If one of these is answered positively, a screening follows which includes surrogate measures of nutritional status, with static and dynamic parameters and data on the severity of the disease (stress metabolism). For each parameter, a score from 0 to 3 can result. Age over 70 years is considered a risk factor and is included in the screening tool, giving 1 point. A total score of =3 points means that the patient is at risk of malnutrition or already malnourished.	1 day (Transfer from the Intensive Care Unit)
Secondary	Albumin in g/dL		1 day (Transfer from the Intensive Care Unit)
Secondary	C-reactive protein in mg/dl		1 day (Transfer from the Intensive Care Unit)
Secondary	Body mass index		1 day (Transfer from the Intensive Care Unit)