To study the effects of a pre-operative supplemental enteral feeding with IMPACT® on the systemic inflammatory response to cardiopulmonary bypass and on immunological parameters will be examined.
ID
Bron
Verkorte titel
Aandoening
High risk patients undergoing elective cardiac surgery.
Ondersteuning
Bern
Switzerland
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Postoperative morbidity, e.g. infectious morbidity & organ (dys)function.
Achtergrond van het onderzoek
Preoperative oral immune enhancing nutritional supplement reduces postoperative infectious morbidity and results in a more stable circulation; the addition of glycine does not result in any benificial effect over standard oral immune enhancing nutritional supplement.
Doel van het onderzoek
To study the effects of a pre-operative supplemental enteral feeding with IMPACT® on the systemic inflammatory response to cardiopulmonary bypass and on immunological parameters will be examined.
Onderzoeksopzet
N/A
Onderzoeksproduct en/of interventie
All patients receive an oral nutritional supplement for at least 5 days with a maximum of 10 days before their operation in addition to their normal diet. One treatment group received a supplement that was enriched with arginine, omega-3 PUFAs and nucleotides compared to the control. The other
treatment group received a supplement that was further enriched with glycine
compared with the first treatment group. Patients that needed enteral nutrition postoperatively received a formula that was comparable with the preoperative supplement.
Algemeen / deelnemers
P.O. Box 22660
Robert Tepaske
Meibergdreef 9
Amsterdam 1100 DD
The Netherlands
r.tepaske@amc.uva.nl
Wetenschappers
P.O. Box 22660
Robert Tepaske
Meibergdreef 9
Amsterdam 1100 DD
The Netherlands
r.tepaske@amc.uva.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Patients aged >= 70 years undergoing coronary bypass grafting, or pre-operative fraction < 0.40 or patients undergoing mitral valve replacements or combinations.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Age <21 years;
2. Pregnancy;
3. Insulin depedent diabetes mellitus;
4. Hepatic cirrhosis;
5. Known malignancy;
6. Use of chemotherapy, NSAIDs or corticosteroids;
7. Schizophrenia;
8. Severe renal failure;
9. Patients with organ transplantation in the past.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL410 |
NTR-old | NTR450 |
Ander register | : 96.17.066 |
ISRCTN | ISRCTN37657221 |
Samenvatting resultaten
<br><br>
Abstract NESPEN, december 2004.<br>