N/A
ID
Bron
Verkorte titel
Aandoening
Acute myeloid leukemia
Acute myeloide leukemie
Ondersteuning
Dept. of Hematology
University Medical Center Groningen
P.O. Box 30.001
9700 RB Groningen
The Netherlands
Phone: +31 50 361 61 61
E-mail: e.vellenga2int.umcg.nl
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. Defining the severity of epithelial dysfunction measured with mucositis score, the stool volume, the calprotectin level in the stool, the urinary Cr EDTA excretion and serum IL-8 and CRP levels;<br>
2. Typhlitis based on clinical symptomatology and CT-scanning abdomen.
Achtergrond van het onderzoek
Rationale:
10-20% of the patients with acute myeloid leukaemia (AML) develop typhlitis following intensive chemotherapy. This might be related to cytotoxic effects of chemotherapy to epithelial and endothelial cells. So far no predictive parameters have been identified that can recognize this subgroup of patients.
Objective:
To identify predictive parameters for typhlitis in AML patients treated with intensive chemotherapy.
Study design:
Pilot study. AML patients that have been treated with intensive chemotherapy will be followed during 14-days following chemotherapy regarding parameters that reflect epithelial damage.
Study population:
1. Patient age 18-70 years;
2. Treated for AML with intensive chemotherapy.
Intervention:
1. Blood and stool samples will be collected;
2. CT-scan of abdomen at day 10-12;
3. Mucositis score will be determined;
4. DNA isolation from normal peripheral blood.
Main study parameters/endpoints:
1. Defining the severity of epithelial dysfunction measured with mucositis score, the stool volume, the calprotectin level in the stool, the urinary Cr EDTA excretion and serum IL-8 and CRP levels;
2. Typhlitis based on clinical symptomatology and CT-scanning abdomen.
Procedure:
1. Sampling blood and stool;
2. CT-scan.
Investigations:
1. Mucositis score; stool volume;
2. Serum IL-8 and CRP levels;
3. Urinary excretion of;
4. CT-scan abdomen;
5. DNA isolation from normal peripheral blood.
Country of recruitment:
The Netherlands.
Doel van het onderzoek
N/A
Onderzoeksopzet
N/A
Onderzoeksproduct en/of interventie
1. Blood and stool samples will be collected;
2. CT-scan of abdomen at day 10-12;
3. Mucositis score will be determined;
4. DNA isolation from normal peripheral blood.
Publiek
P.O. Box 30001
E. Vellenga
Groningen 9700 RB
The Netherlands
+31 (0)50 3612354
e.vellenga@int.umcg.nl
Wetenschappelijk
P.O. Box 30001
E. Vellenga
Groningen 9700 RB
The Netherlands
+31 (0)50 3612354
e.vellenga@int.umcg.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Age 18-70 years;
2. Diagnosed with AML and treated with intensive chemotherapy.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Ineligible to perform the tests.
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 | NL692 |
NTR-old | NTR1800 |
Ander register | MEC UMCG : 2008/113 |
ISRCTN | ISRCTN wordt niet meer aangevraagd |