Can IV nutrition at an outpatient clinic help malnourished surgery patients?
NCT ID NCT03926949
First seen Sep 11, 2026 ยท Last updated Sep 11, 2026
Summary
Malnutrition is common in people having major surgery and links to worse outcomes. This study tests whether malnourished patients can receive intravenous nutrition, a mix of carbohydrates, fats, and protein, at an outpatient clinic for 5 to 10 days before surgery instead of being admitted to hospital. Researchers will track how many patients complete the nutrition plan and whether they have fewer complications after surgery. The study includes 13 adults identified as malnourished by a screening tool and a nutrition assessment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Parenteral nutrition, an intravenous mixture of carbohydrates, fats, and protein given through a vein
- What this could lead to
- If it works, this could offer a way to give malnourished patients intravenous nutrition before surgery without admitting them to hospital, which may free up beds and lower costs.
- What could go wrong
- This is a small feasibility study with 13 participants, so it can only show whether the approach is practical, not whether it improves outcomes. Intravenous nutrition carries risks such as infection and blood sugar problems, and the results may not apply to other hospitals or patient groups.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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13 people
The number who actually took part.
- Started
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Oct 2019
- Finished
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Jul 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients 18 years of age or older 2. Patients screened at risk of malnutrition by Canadian Nutrition Screening Tool (CNST) and identified as malnourished by subjective global assessment (SGA) B or C Exclusion Criteria: 1. Patients undergoing minor or laparoscopic surgery 2. Pregnancy 3. Patients with severe systemic diseases defined by American Society of Anesthesiologists (ASA) classification III to V 4. Patients with diabetes mellitus 5. Patients with planned palliative treatment
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Royal Alexandra Hospital
Edmonton, Alberta, T5H 3V9, Canada
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University of Alberta Hospital
Edmonton, Alberta, T6G 2B7, Canada
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