Trials / Completed
CompletedNCT00730808
Effectiveness and Tolerability of an Oral Nutritional Supplement (PreOP Booster) Given Before Surgery
Efficacy and Tolerability of a Preoperative Oral Nutritional Supplement (PreOP Booster) vs. Placebo in Surgical Patients (Pilot Study)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Fresenius Kabi · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this pilot study is to investigate effectiveness, tolerability and safety of an oral nutritional supplement (PreOP Booster), given to rectal tumour patients prior to low anterior resection.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | PreOP Booster (food for special medical purposes) | 3x1 dosage is given prior to surgery: 2x1 the day prior to surgery; 1x1 3-4h prior to initiation of anaesthesia; |
Timeline
- Start date
- 2008-12-01
- Primary completion
- 2009-11-01
- Completion
- 2009-11-01
- First posted
- 2008-08-08
- Last updated
- 2010-05-19
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT00730808. Inclusion in this directory is not an endorsement.