Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
550 participants
OBSERVATIONAL
2016-01-01
2021-08-14
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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With glutamine supplementation
perioperative glutamine supplementation (PGS) was defined as the subjects with five-day parenteral plus one-month oral use.
SYMPT-X Glutamine, Oral Powder for Reconstitution
erioperative glutamine supplementation (PGS) was defined as the subjects with five-day parenteral plus one-month oral use.
Without glutamine supplementation
no glutamine use
SYMPT-X Glutamine, Oral Powder for Reconstitution
erioperative glutamine supplementation (PGS) was defined as the subjects with five-day parenteral plus one-month oral use.
Interventions
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SYMPT-X Glutamine, Oral Powder for Reconstitution
erioperative glutamine supplementation (PGS) was defined as the subjects with five-day parenteral plus one-month oral use.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
20 Years
ALL
No
Sponsors
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National Taiwan University Hospital
OTHER
Responsible Party
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Other Identifiers
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201909033RIND
Identifier Type: -
Identifier Source: org_study_id
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