Study of Postoperative Nutritional Support in Cardiac Surgery.
This study is currently recruiting participants.
Verified December 2012 by Meshalkin Research Institute of Pathology of Circulation
Sponsor:
Meshalkin Research Institute of Pathology of Circulation
Information provided by (Responsible Party):
Efremov Sergey, Meshalkin Research Institute of Pathology of Circulation
ClinicalTrials.gov Identifier:
NCT01312870
First received: March 2, 2011
Last updated: December 19, 2012
Last verified: December 2012
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Purpose
The purpose of this study is to determine whether postoperative nutritional support improves postoperative outcomes in cardiac patients with malnutrition .
| Condition | Intervention | Phase |
|---|---|---|
|
Heart Diseases |
Dietary Supplement: Ensure, Abbott Nutrition Other: standard hospital diet |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Prospective Randomized Study of Postoperative Nutritional Support in Cardiac Surgery. |
Resource links provided by NLM:
Further study details as provided by Meshalkin Research Institute of Pathology of Circulation:
Primary Outcome Measures:
- Mortality [ Time Frame: 1 month ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Postoperative complications [ Time Frame: 1 month ] [ Designated as safety issue: No ]Cardiac arrhythmia, infectious complications.
- Total lymphocyte count [ Time Frame: before operation, 7, 14, 21 postoperative days ] [ Designated as safety issue: No ]
- Serum albumin [ Time Frame: Before operation, 7, 14, 21 postoperaitve days ] [ Designated as safety issue: No ]
- Serum prealbumin [ Time Frame: Before operation, 7, 14, 21 postoperaitve days ] [ Designated as safety issue: No ]
- Retinol-binding protein [ Time Frame: Before operation, 7, 14, 21 postoperaitve days ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 200 |
| Study Start Date: | March 2011 |
| Estimated Primary Completion Date: | February 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: postoperative nutritional supplements
postoperative nutritional supplements in addition to standard hospital diet
|
Dietary Supplement: Ensure, Abbott Nutrition
Enteral feeding Ensure, Abbott Nutrition 400 ml per day for seven postoperative days
|
|
Placebo Comparator: standard hospital diet
patients receiving standard hospital diet
|
Other: standard hospital diet
standard hospital diet
|
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Absolute lymphocyte count < 1500
- Albumin <35 g/L
- Body mass index<21 kg/m2
- "B" class of nutritional status according to Subjective Global Assessment
Exclusion Criteria:
- Hepatitis B, C
- Total circulatory arrest
- Absence of informed consent signed
- Chronic liver diseases
- Gastric resection in patient's history
- Physical limitations of normal feeding
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01312870
Contacts
| Contact: Vladimir Lomivorotov, MD, PhD | vvlom@mail.ru | |
| Contact: Sergey Efremov, MD, PhD | sergefremov@mail.ru |
Locations
| Russian Federation | |
| State Research Institute of CIrculation Pathology Novosibirsk, Russian Federation | Recruiting |
| Novosibirsk, Russian Federation | |
| State Research Institute of CIrculation Pathology | Not yet recruiting |
| Novosibirsk, Russian Federation | |
| Contact: Vladimir Lomivotov, MD, Prof. vvlom@mail.ru | |
| Principal Investigator: Vladimir Lomivorotov, MD, PhD | |
| Sub-Investigator: Sergey Efremov, MD, PhD | |
| Sub-Investigator: Alexandr Svyatchenko | |
Sponsors and Collaborators
Meshalkin Research Institute of Pathology of Circulation
More Information
No publications provided
| Responsible Party: | Efremov Sergey, Anesthesist, Meshalkin Research Institute of Pathology of Circulation |
| ClinicalTrials.gov Identifier: | NCT01312870 History of Changes |
| Other Study ID Numbers: | PNSICP-71421 |
| Study First Received: | March 2, 2011 |
| Last Updated: | December 19, 2012 |
| Health Authority: | Russia: Ethics Committee |
Additional relevant MeSH terms:
|
Heart Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on June 18, 2013