A Comparative Evaluation of Mosapride Versus Metoclopramide for Enteral Feeding Intolerance in Critically Ill Patients

Phase 3

Not yet recruiting

• Conditions: Enteral Feeding Intolerance
• Interventions: Drug: Mosapride Citrate Tablets; Drug: Metoclopramide 10mg

• Registration Number: NCT06826443
• Lead Sponsor: Ain Shams University

Brief Summary

Caring for critically ill patients in an intensive care unit (ICU) is considered a standard of care. According to the Society of Critical Care Medicine (SCCM), as a function of the complex nature of the care provided in the ICU, the ideal method to provide support to the critically ill involves the participation of a multi-professional staff.

Provision of nutrition support to the critically ill is now established as an essential part of patient care where aiming toward 100% of the predicted target may have resulted in reduced mortality and increased ventilator-free days in those who are premorbid malnourished. Despite these reported benefits, clinicians continue to deliver little more than half of the enteral nutrition (EN) they plan to provide, due to gastric motility disorders, patient intolerance and clinical interruptions. Also despite the availability of numerous clinical practice guidelines (CPGs) focused on feeding critically ill patients, observational studies have consistently demonstrated persistent and significant gaps between guideline recommendations and actual nutrition practice. Consequently, underfeeding is prevalent in the intensive care unit (ICU), with patients on average receiving only 60 % of the calories that are prescribed. Moreover, Among the barriers to adequate nutritional supply in the ICU which contributes to nutritional status deterioration, gastrointestinal disorders causing enteral feed intolerance are the most important and the most often mentioned in the literature. when gastric emptying was measured in critically ill patients, 46 % of them had evidence of delayed gastric emptying. Untreated slow gastric emptying has a plethora of clinical consequences such as vomiting, aspiration of gastric contents, pneumonia, and contributes significantly to the frequent interruptions and cessation of EN in the ICU, which results in inadequate nutritional delivery. Studies have shown an association between feeding intolerance, prolonged intensive care unit (ICU) stay, and increased risk of death.

Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patients has demonstrated the importance of the use of prokinetic drugs to improve tolerance to gastric feeding in critically ill patients and achieve earlier discharge.

Prokinetic drugs act by promoting gastric motility, increase gastric emptying, prevent the retention and reflux of gastric contents and thus provide symptomatic relief.

Most of the prokinetic drugs are efficacious with prokinetic activity but the matter of major concern is their side effect profile. The most commonly used agent is metoclopramide. Although it is the most commonly used prokinetic to treat delayed gastric emptying and facilitate early enteral feeding, adverse complications limit its use including tachyphylaxis, tardive dyskinesia on long term use and QT prolongation predisposing to cardiac arrhythmias. Several drug targets have been identified to develop new promotility agents and several new medications are under investigation to overcome the side effects caused by most of the prokinetics .

Mosapride is another available prokinetic agent that enhances gastric motility through serotonin receptor agonism; resulting in prokinetic effects. It accelerates gastric emptying, improves gastric tension and sensitivity, and has anti-emetic action.

The aim of the current study is to compare the effectiveness as well as the safety of Mosapride against metoclopramide as the first line treatment for feeding intolerance in critically ill patients.

Detailed Description

Not available

Study Timeline

• Status Verified: 2025-02
• Study Start: 2025-02
• Study First Submitted: 2025-02-06
• Study First Submitted QC: 2025-02-12
• Last Update Submitted: 2025-02-13
• Study First Posted: 2025-02-14
• Last Update Posted: 2025-02-17
• Primary Completion: 2025-05
• Study Completion: 2025-05

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• Patients aging between 18 and 60 years (of both sexes)
• Patients admitted to the ICU and are expected to stay in the ICU for not less than 7 days
• Patients prescribed enteral feeding.

Exclusion Criteria

The following patients are

• Age less than 18 years or more than 60 years.
• Patients who had previous upper gastrointestinal tract surgery, obstruction, hemorrhage or history of GI disease.
• Patients who are clinically significant hepatic dysfunction. (>3 times above the upper end of normal range of bilirubin, γ-glutamyl transferase, aspartate transaminase, or lactate dehydrogenase)
• Patients who are on regular use of H2 blockers, prokinetic, proton pump inhibitor or anticholinergic agents for previous 4 weeks.
• Patients with arrhythmia or atrioventricular blocks.
• Patients with any condition or comorbid disease that might interfere with gastric emptying such as diabetes.
• Patients with head injuries.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Mosapride citrate group	Mosapride Citrate Tablets	These patients will receive Mosapride citrate (5 mg) three times daily for 7 days.
Metoclopramide	Metoclopramide 10mg	These patients will receive metoclopramide (10 mg) three times daily for 7 days.

Primary Outcome Measures

Name	Time	Method
Gastric residual volume will be measured by ultrasonography	GRV will be measured daily for the duration of therapy which is 7 days	the gastric residual volume will be assessed by ultrasonography on daily basis for the duration of the study period

Secondary Outcome Measures

Name	Time	Method
Incidence of infectious complications such as pneumonia or any other infection complication will be assessed throughout the study period	Incidence of infectious complications will be assessed for the 7 days study period
Length of intensive care unit (ICU) stay will be assessed from the day of admission to ICU till the day of discharge from ICU	Length of ICU stay will be assessed from the day of admission to the ICU till the day of discharge from ICU
Any Adverse drug event as abdominal pain, QT prolongation and cardiac side effects that occur within the study period will be recorded throughout the study period	adverse drug events will be recorded for the study period of 7 days
Determining the adequacy of enteral nutrition will be assessed by measuring the enteral nutrition volume ratio at base line and at the end of the study period	Determining the adequacy of enteral nutrition will be assessed on daily base for the duration of study period of 7 days	the adequacy of enteral nutrition will be assessed by measuring the enteral nutrition volume ratio (the ratio of the actual received to the prescribed enteral nutrition volume ) at baseline of the study and at the end of the study.

Trial Locations

Locations (1)

Matarya Teaching Hospital; 🇪🇬 Cairo, Egypt