Food for Special Medical Purpose in Patients With Digestive Tract Tumor
Study Details
Study Description
Brief Summary
This is a prospective, randomized, controlled, unblinded, parallel, multicenter, and non-inferiority study to demonstrate the safety and efficacy of a Food for Special Medical Purpose product (FSMP) in participants with digestive tract tumor undergoing surgical resection during the perioperative period.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
This is a prospective, randomized, controlled, unblinded, parallel, and multicenter, and non-inferiority study to demonstrate the safety and efficacy of a FSMP in participants with digestive tract tumor undergoing surgical resection during the perioperative period. Half of the participants will receive FSMP, the other half will receive Enteral Nutrition Emulsion (TPF-T) as an active control.
Prealbumin, albumin, C-reactive protein (CRP), immunology parameters, vital signs, nutrition and safety-related laboratory parameters, compliance, and Adverse Events (AEs) will be evaluated in this study, to demonstrate its parity with TPF-T on efficacy and safety.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Experimental Product Food for Special Medical Purpose (FSMP) is a special medical food for patients with tumors |
Other: Experimental Product
Before the surgery: FSMP provides daily target energy needed by participants
1-2 days after surgery: Start FSMP and advance as tolerated to achieve 20% of the daily target energy needed by participants
3rd-5th day after surgery: Gradually increase FSMP intake every day as tolerated to provide 30-80% of the daily target energy needed by participants
6th day after surgery to final visit: FSMP provides daily target energy needed by participants
|
| Active Comparator: Control Product Nutrition Emulsion (TPF-T) TPF-T is a tumor-specific enteral nutrition therapy |
Other: Control Product
Before surgery: TPF-T provides daily target energy needed by participants
1-2 days after surgery: Start TPF-T and advance as tolerated to achieve 20% of the daily target energy needed by participants
3rd-5th day after surgery: Gradually increase TPF-T intake every day as tolerated to provide 30-80% of the daily target energy needed by participants
6th day after surgery to final visit: TPF-T provides daily target energy needed by participants
|
Outcome Measures
Primary Outcome Measures
- Serum Pre-Albumin [Baseline to Post Op Day (POD) 8]
Change in pre-albumin
Secondary Outcome Measures
- Serum Albumin [Baseline to Post Op Day (POD) 8]
Change in albumin
- Weight [Baseline to Post Op Day (POD) 8]
Change in weight
- Nutritional Risk Screening (NRS) 2002 [Baseline to Post Op Day (POD) 8]
NRS-2002 scored from 0 Low Risk to 7 High Risk
- Patient-Generated Subjective Global Assessment (PG-SGA) [Baseline to Post Op Day (POD) 8]
PG-SGA scored from 0 to 9 or greater; higher score indicates nutrition intervention recommendation
Other Outcome Measures
- C-reactive Protein (CRP) [Baseline to Post Op Day (POD) 8]
Change in CRP
- Length of hospital stay [From Date of Admission until Date of Discharge, typically up to 14 days]
Days stay in hospital
- Hand Grip Strength [Baseline to Post Op Day (POD) 8]
Measured in kg
- Eastern Cooperative Oncology Group (ECOG) Performance Status [Baseline to Post Op Day (POD) 8]
Healthcare Professional assessed score with range from 0 to 5; higher scores indicate worsening functional status
- Product Intake [Baseline to Post Op Day (POD) 8]
Daily volume of study product consumed
- Adverse Events [Baseline to Post Op Day (POD) 8]
Reported adverse events for assessment of safety and tolerability
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Participant is male or female, between 18 and 75 years old, female participant is non-pregnant or non- lactating, at least 6 weeks postpartum
-
Participants with digestive tract tumors diagnosed by histological method or radiological diagnosis and scheduled to undergo surgical resection
-
Participant with NRS-2002 score ≥3
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Participant is willing to comply with the study protocol, able and willing to consume study product according to the protocol
-
Participants with Body Mass Index 18.5 - 30 kg/m2
-
Participant has voluntarily signed and dated an informed consent form (ICF), approved by an Institutional Review Board (IRB) / Independent Ethics Committee (IEC) prior to any participation in the study
Exclusion Criteria:
-
Participant has an expected life expectancy < 3 months
-
Participant has contraindications to enteral nutrition (such as active gastrointestinal hemorrhage, bowel obstruction, decompensated short bowel syndrome, high flow intestinal fistula, severe intraperitoneal infection, severe gastrointestinal emptying disorder, unstable vital signs, dyscoagulation, severe nausea, vomiting and/or uncontrolled diarrhea/steatorrhoea) that in the opinion of the study physician cannot be corrected
-
Participant had plasma infused, RBC infused, albumin infused, amino acid infused or undergone radiotherapy and/or chemotherapy within 1 week before screening
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Participant with serum Albumin <2.5g/dl at the time of the screening
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Participant has moderate to severe anemia, i.e. Hgb < 90g / L
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Patients who plan to receive endoscopic tumor resection or / and palliative surgery
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Participant has renal dysfunction (serum creatinine > 2 times the upper limit of normal (ULN))
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Participant has liver insufficiency [serum alanine transaminase (ALT) and/or aspartate transaminase (AST) > 2 times the ULN or severe cholestasis (conjugated bilirubin > 2 times the ULN)]
-
Participant has severe cardiac insufficiency (e.g., Severe arrhythmia or atrial fibrillation; myocardial ischemia or stent surgery with unstable cardiac function within 3 months prior to screening visit )
-
Participant states that he/she has had a significant cardiovascular and cerebrovascular event (e.g., myocardial infarction, stroke) within six months prior to screening visit; or stated history of congestive heart failure
-
Participant with type I diabetes, or type II diabetes with fasting blood glucose ≥8mmol/L
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Participant has history of significant neurological or psychiatric disorder
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Participant has history of alcoholism, drug abuse or other conditions that may interfere with study product consumption or compliance with study protocol procedures
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Participant has a known history of allergy or intolerance to any ingredient in the investigational products
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Participant is currently undergoing tumor immunotherapy taking medications/substances that could profoundly modulate appetite, metabolism or inflammatory level
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Appetite enhancers, pregnancy promoters, steroids (nasal inhalation, topical and optical steroids are acceptable);
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Anti-inflammatory fat emulsions or other oral nutritional supplementations/drugs containing Omega-3 fatty acids, protein, glutamine, or arginine.
-
Dexamethasone, growth hormone or other drugs affecting metabolism;
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Participant is currently undergoing tumor immunotherapy or taking medications/substances that could profoundly modulate immune function, such as PD1 or PDL1 inhibitors; CTLA-4 inhibitor; Thymosin; Azathioprine; Cyclosporine; Tacrolimus; Tumor necrosis factor antagonist; Lentinan; immune-modulating Chinese medicine
-
Participant with active tuberculosis and HIV infection
-
Participant participated in any clinical trial within four weeks prior to the screening visit.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Beijing Hospital | Beijing | China | 100005 | |
| 2 | Peking Union Medical College Hospital | Beijing | China | 100005 | |
| 3 | Peking University People's Hospital | Beijing | China | 100044 | |
| 4 | Beijing Cancer Hospital | Beijing | China | 100142 | |
| 5 | Beijing Tsinghua Changgung Hospital | Beijing | China | 102218 | |
| 6 | The Six Afffilated Hospital Sun Yat-sen University | Guangzhou | China | 510665 | |
| 7 | The Affiliated Hospital of Qingdao University | Qingdao | China | 266003 | |
| 8 | Zhongshan Hospital Affiliated to Shanghai Fudan University | Shanghai | China | 200031 | |
| 9 | Renji Hospital Shanghai Jiaotong University School of Medicine | Shanghai | China | 200127 |
Sponsors and Collaborators
- Abbott Nutrition
Investigators
- Study Chair: Fei Li, PhD, Abbott Nutrition
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- BL43