Omega-3 vs Very Low Calorie Diet for Liver Size Reduction
Obesity, Morbid, Obesity, NAFLD
About this trial
This is an interventional treatment trial for Obesity, Morbid
Eligibility Criteria
Inclusion Criteria:
Participants must meet ALL of the following inclusion criteria:
- Fulfilled criteria for bariatric surgery as coined by National Institutes of Health conference (a body mass index (BMI) of 40 or more, OR a BMI of 35 or more with a serious health problem linked to obesity, such as type 2 diabetes, heart disease, or sleep apnea)
- Their age is ≥18 years and ≤70 years
- Able and willing to give written consent
- The patient is willing to perform the pre-operative tests required for this study.
Exclusion Criteria:
Participants who meet any of the following criteria at the time of the baseline visit are NOT eligible to be enrolled in this study:
- Prior bariatric surgery
- Patient must not have any acute or chronic alteration of liver function (i.e. cirrhosis, active or chronic hepatitis, congenital hepatic disease, etc.)
- Prior hepatic surgery
- Contra-indication to general anesthesia
- Any medical condition, which in the judgement of the Investigator and/or designee makes the subject a poor candidate for the investigational procedure
- Pregnant or lactating female (Women of child bearing potential must take a pregnancy test prior to surgery)
- Patients receiving medication that would alter hepatic function significantly.
- Patients with ascites.
- History of alcohol abuse: >3 standard drinks/day in men or >2 standard drinks/day in women (one standard drink being defined as 12 ounces of 5% beer, 5 ounces of 12% wine or 1.5 ounces of 40% liquor).
- Patients consuming Ω-3 supplements on a regular basis.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Experimental
No Intervention
Very Low Calorie Diet
Omega-3
No-treatment
The first group will continue according to the standard bariatric preoperative protocol and will be assigned a VLCLD of 900 cal/day (Optifast ® 4 servings/day each containing: 225 cal + 0.35 g linolenic acid) for 2-3 weeks prior to surgery according to the surgeon's preferences.
The second group will be assigned to 3 gr. daily oral intake of Ω-3 PUFAs ((Oceano3 ® 1000 mg Krill Oil tabs (150 mg EPA + 90 mg DHA) 3 times a day) for 4 weeks with only regular dietary suggestions before surgery.
The third group will not receive treatment for liver size reduction prior to surgery.