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Assessment of a low energy diet using meal replacements before surgery for weight loss

Evaluation of a pre-operative meal replacement program in bariatric surgery patients

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12611000258954
Enrollment
30
Registered
2011-03-09
Start date
2011-05-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The purpose of this study is to assess the effect of the pre-operative very low energy diet on liver function tests and weight loss, and to correlate these outcomes with compliance to the program. Our hypotheses are: 1. Pre-operative weight loss will be associated with an improvement in liver function tests 2. Increased compliance to the program will be associated with greater weight loss

Interventions

As part of usual care, patients will be advised to consume 2 commercially available meal replacements, either a shake or a bar, for two meals a day and a commercially available energy controlled normal meal for one meal a day. Patients will also be advised about fruit and vegetable intake and recommended to have two and five serves respectively. Duration of the diet will be prescribed on an individual basis for between 2-6 weeks prior to surgery. The overall duration of the study will be six m

As part of usual care, patients will be advised to consume 2 commercially available meal replacements, either a shake or a bar, for two meals a day and a commercially available energy controlled normal meal for one meal a day. Patients will also be advised about fruit and vegetable intake and recommended to have two and five serves respectively. Duration of the diet will be prescribed on an individual basis for between 2-6 weeks prior to surgery. The overall duration of the study will be six months. Patients will be recruited as they are assessed as being eligible for surgery. Each patient will be observed for up to six weeks.

Sponsors

University of South Australia
Lead SponsorUniversity

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Body Mass Index (BMI) > 40 kg/m2 or > 35 kg/m2 and one obesity related illness/comorbidity

Exclusion criteria

Not suitable for bariatric surgery

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026