Unique ID issued by UMIN | UMIN000036440 |
---|---|
Receipt number | R000041522 |
Scientific Title | Study to estimate the efficacy of heat-killed Lactobacillus (K15) to privent infection in infant after discharge from NICU or GCU; double-blind, randomized controlled trial |
Date of disclosure of the study information | 2019/04/08 |
Last modified on | 2024/07/03 13:50:49 |
Study to estimate the efficacy of heat-killed Lactobacillus (K15) to privent infection in infant after discharge from NICU or GCU; double-blind, randomized controlled trial
Study to estimate the efficacy of heat-killed Lactobacillus (K15) to privent infection in infant after discharge from NICU or GCU; double-blind, randomized controlled trial
Study to estimate the efficacy of heat-killed Lactobacillus (K15) to privent infection in infant after discharge from NICU or GCU; double-blind, randomized controlled trial
Study to estimate the efficacy of heat-killed Lactobacillus (K15) to privent infection in infant after discharge from NICU or GCU; double-blind, randomized controlled trial
Japan |
infants who were born within gestational age of 35 weeks or less and were treated in and discharged from NICU or GCU
Pediatrics |
Others
NO
The purpose of this study is to estimate the efficacy of heat-killed K15 to prevent virus respiratory tract infections in premature infants who were treated in and discharged from NICU or GCU
Safety,Efficacy
duration of fever episodes
1. frequency of respiratory tract infection
2. severity of respiratory tract infection
3. frequency of Respiratory syncytial virus (RSV) infection diagnosed by physician
4. Severity of respiratory disorder
5. Serum IgG, IgA, IgM before and after treatment
6. side effects related to K15 administration
Interventional
Parallel
Randomized
Individual
Double blind -all involved are blinded
Placebo
2
Prevention
Medicine |
administer 4.6mg of K15 (adjusted to total 100mg with dextrin) once daily from the first outpatient visit to 12 months orally or by tube
administer placebo (100mg of dextrin) once daily from the first outpatient visit to 12 months orally or by tube
Not applicable |
Not applicable |
Male and Female
1) infants who were born within gestational age of 35 weeks or less and were treated in and discharged from NICU or GCU
2) Signed consent form to participate in the study was obtained from the infant's legal representative (guardian) by her/his free will after full explanation of this study
1) infants who have allergy to Lactobacillus preparation or products derived from soy
2) infants who have congenital heart defect, severe respiratory disorder, chromosomal abnormality, or primary immunodeficiency
3) infants who are considered unsuitable to participate in this study by attending physician
70
1st name | Naoki |
Middle name | |
Last name | Shimojo |
Chiba University
Graduate School of Medicine
260-0856
1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba, 260-8670, JAPAN
043-226-2144
shimojo@faculty.chiba-u.jp
1st name | Hiroki |
Middle name | |
Last name | Takayama |
Soiken Inc.
Clinical Study Support Division
101-0052
NBF Ogawamachi Building 4F, 1-3-1 Ogawamachi, Kanda, Chiyoda-ku, Tokyo. 101-0052, JAPAN
03-3295-1350
takayama@soi-kenkyu.com
Graduate School of Medicine, Chiba University
Kikkoman Corporation
Profit organization
Chiba University Hospital Ethics Review Board
1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba, 260-8670, JAPAN
043-222-7171
chibacrc@mac.com
NO
2019 | Year | 04 | Month | 08 | Day |
Unpublished
No longer recruiting
2018 | Year | 12 | Month | 13 | Day |
2019 | Year | 02 | Month | 28 | Day |
2019 | Year | 02 | Month | 28 | Day |
2021 | Year | 12 | Month | 31 | Day |
2019 | Year | 04 | Month | 08 | Day |
2024 | Year | 07 | Month | 03 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041522