Effects of Nutritional Preconditioning on the Patient's Outcomes After Surgery

NCT ID: NCT03692507

Last Updated: 2021-07-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-07-30

Study Completion Date

2022-12-30

Brief Summary

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Malnutrition is a serious problem in patients undergoing major surgeries and has a direct association with increased morbidity, mortality, length of stay (LOS), increased readmissions and cost of care. Studies suggest several advantages of supplementation with protein or specific amino acids in malnourished patients. Dietary leucine or its metabolite β-hydroxy β-methylbutyrate (HMB) can improve skeletal muscle mass and function by increasing transcriptional level of protein synthase, while other high protein or amino acids like Glutamine or Arginine supplements only provide protein-amino acids pool for patients while body's preferred fuel during metabolic stress is endogens protein, rather than exogenous diet.

In this study the investigators seek to achieve two distinct goals:

1. Determine the patients' nutritional status before and after major surgeries by baseline and subsequent nutritional assessments, according to ASPEN's criteria. In addition, the investigators were going to use indirect calorimetry to determine the Resting Energy Expenditure (REE) in different phases of pre- and postoperative periods. The investigators also propose to compare different serum protein markers and their ratios in order to correlate them with ASPEN's criteria for nutritional status quantification. In Summary, three discrete tools including ASPEN's criteria, indirect calorimetry, and serum biomarkers are going to be used in conjunction with each other to delineate the patients' nutritional status in various pre- and post-operative periods.
2. Patients undergoing major surgeries were supplemented with high protein with ß-hydroxy ß-methylbutyrate (HMB) (Ensure, Envile) or HMB only as a control, in order to improve their nutritional status and improve postoperative outcomes. The investigators looked for depict meaningful improvements in surgical outcomes by nutritional supplementation with or without HMB.

Detailed Description

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Hypotheses:

We hypothesize that patients receiving high protein nutritional supplementation with HMB (Ensure Enlive) will have meaningful improvements in surgical outcomes rather than if they receive HMB only. Also, by comparing different methods of malnutrition designation, we are hypothesizing that by conduction this study, we will have a better understanding of malnutrition and its consequences in the Central Valley of California. Furthermore, we are planning to improve patient outcomes and significantly reduce the health care costs of the Valley by proper nutritional supplementation.

Specific Aims:

Demonstrate the important role β-hydroxy β-methyl butyrate (HMB) supplementation with or without high protein nutrition supplement in patients undergoing major surgeries and their outcomes.

Develop the current ERAS protocol used in Community Regional Medical Center by determining the best oral nutrition supplement prior to surgery Emphasize the importance of using oral nutrition supplements before major surgeries to decrease the patient's recovery after surgeries.

Conditions

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Major Abdominal/GI Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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HMB only

Taking HMB supplements three times a day

Group Type EXPERIMENTAL

HMB

Intervention Type DIETARY_SUPPLEMENT

Patients in the first group (HMB only) will take 3 capsules of HMB by VitaMonk™ (1000mg/capsule) daily (morning, noon, and night) for 5 days prior to surgery.

Protein and HMB

Drinking Ensure Enlive shakes

Group Type EXPERIMENTAL

Protein and HMB

Intervention Type DIETARY_SUPPLEMENT

Patients in the second group (HMB + protein) will drink 2- 8oz bottles of Ensure Enlive daily (morning and night) for 5 days prior to surgery. Each bottle contains 1500mg of HMB and 20 g of protein.

Current ERAS (High Protein)

Drinking Ensure surgery shakes + Ensure pre-surgery

Group Type EXPERIMENTAL

ERAS

Intervention Type DIETARY_SUPPLEMENT

Patients in the third group (High protein) will drink 2- 8oz bottles of Ensure surgery daily (morning and night) for 5 days prior to surgery. Each bottle contains 18g of protein. and a clear 50g Pre-surgery drink on the day of surgery

Interventions

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HMB

Patients in the first group (HMB only) will take 3 capsules of HMB by VitaMonk™ (1000mg/capsule) daily (morning, noon, and night) for 5 days prior to surgery.

Intervention Type DIETARY_SUPPLEMENT

Protein and HMB

Patients in the second group (HMB + protein) will drink 2- 8oz bottles of Ensure Enlive daily (morning and night) for 5 days prior to surgery. Each bottle contains 1500mg of HMB and 20 g of protein.

Intervention Type DIETARY_SUPPLEMENT

ERAS

Patients in the third group (High protein) will drink 2- 8oz bottles of Ensure surgery daily (morning and night) for 5 days prior to surgery. Each bottle contains 18g of protein. and a clear 50g Pre-surgery drink on the day of surgery

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

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Protein

Eligibility Criteria

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Inclusion Criteria

* Dr. Amir Fathi as attending surgeon
* Adult patients (age \>18) undergoing major abdominal and GI surgeries
* Patients at risk for malnutrition based on the ASPEN and The Academy malnutrition criteria

Exclusion Criteria

* Pediatric patients
* Patients undergoing chemotherapy or radiation
* Patients with known allergies to products (Ensure Enlive, HMB)
* Patients that are unable to comply with all requirements
* Vegan patients
* Pregnant patients
* Prisoners
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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California State university, Fresno, Department of Food Science and Nutrition

OTHER

Sponsor Role collaborator

University of California, San Francisco

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Amir h Fathi, MD

Role: PRINCIPAL_INVESTIGATOR

University of California, San Francisco

Locations

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Community Regional Medical Center

Fresno, California, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Amir H Fathi, MD

Role: CONTACT

(559) 256-5140

Shabnam Pooya, PhD

Role: CONTACT

9099915887

Facility Contacts

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Amir Fathi, Co-PI

Role: primary

559-256-5140

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Other Identifiers

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2018006

Identifier Type: -

Identifier Source: org_study_id

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