No registrations found.
ID
Source
Brief title
Health condition
Acute myeloid leukemia
Acute myeloide leukemie
Sponsors and support
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
Intervention
Outcome measures
Primary outcome
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.
Secondary outcome
Before and after treatment with chemo different parameters will be examined.
Background summary
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.
Study objective
N/A
Study design
N/A
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.
P.O. Box 30001
E. Vellenga
Groningen 9700 RB
The Netherlands
+31 (0)50 3612354
e.vellenga@int.umcg.nl
P.O. Box 30001
E. Vellenga
Groningen 9700 RB
The Netherlands
+31 (0)50 3612354
e.vellenga@int.umcg.nl
Inclusion criteria
1. Age 18-70 years;
2. Diagnosed with AML and treated with intensive chemotherapy.
Exclusion criteria
Ineligible to perform the tests.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL692 |
NTR-old | NTR1800 |
Other | MEC UMCG : 2008/113 |
ISRCTN | ISRCTN wordt niet meer aangevraagd |