NCT00365768 · STUDY IN CONTEXT
Glutamine in Treating Neuropathy Caused by Vincristine in Young Patients With Lymphoma, Leukemia, or Solid Tumors
Draft scope assessment: narrower. Linked by condition-string match at the cancer-entity level. The study's eligibility - stage, biomarker, treatment line and prior therapy - has not been reconciled against this page's definition, so its population is narrower than this page in ways not yet recorded. Found by searching ClinicalTrials.gov for this cancer type, restricted to studies that have posted results to the registry. No FDA notice, FDA label or NCI summary held by this site cites this study. Because the search asked for posted results, studies without posted results were never looked for, so their absence from this page means nothing.
Read the full study record and all posted results →
Linked outcomes
Reported safety
Quality of life and patient-reported measures
No linked quality-of-life measure is recorded for this setting and study.
Full draft applicability and source-link record
- trial
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- trial label
- Glutamine in Treating Neuropathy Caused by Vincristine in Young Patients With Lymphoma, Leukemia, or Solid Tumors
- applicability
- narrower
- applicability note
- Linked by condition-string match at the cancer-entity level. The study's eligibility - stage, biomarker, treatment line and prior therapy - has not been reconciled against this page's definition, so its population is narrower than this page in ways not yet recorded.
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- provenance class
- registry-condition-search
- discovery note
- Found by searching ClinicalTrials.gov for this cancer type, restricted to studies that have posted results to the registry. No FDA notice, FDA label or NCI summary held by this site cites this study. Because the search asked for posted results, studies without posted results were never looked for, so their absence from this page means nothing.
- outcome Count
- 2
- harms Count
- 2
- qol Count
- 0
- outcomes
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- outcome key
- om-0000
- source section id
- NCT00365768-om-0000
- source outcome index
- 0
- endpoint
- Incidence of Vincristine-induced Peripheral Neuropathy
- endpoint definition
- Incidence of Vincristine-induced Peripheral Neuropathy
- time origin
- Up to 30 weeks from baseline while on Vincristine treatment
- analysis role
- primary
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- Source null
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- outcome key
- om-0001
- source section id
- NCT00365768-om-0001
- source outcome index
- 1
- endpoint
- Number of Participants With Progression of Neuropathy
- endpoint definition
- Number of Participants With Progression of Neuropathy
- time origin
- 42 days
- analysis role
- secondary
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- Source null
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- arms
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- outcome key
- om-0000
- arm key
- OG000
- arm label
- Arm I: Glutamine
- regimen
- Beginning 1 week after administration of vincristine chemotherapy, patients receive oral glutamine twice daily on days 1-21. Glutamine: Administered orally twice daily for 21 days
- analyzed count
- 24
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00365768-om-0000#groups/OG000
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- outcome key
- om-0000
- arm key
- OG001
- arm label
- Arm II: Placebo
- regimen
- Beginning 1 week after administration of vincristine chemotherapy, patients receive oral placebo twice daily on days 1-21. Placebo: Administered orally twice daily for 21 days
- analyzed count
- 25
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00365768-om-0000#groups/OG001
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- outcome key
- om-0001
- arm key
- OG000
- arm label
- Arm I: Glutamine
- regimen
- Beginning 1 week after administration of vincristine chemotherapy, patients receive oral glutamine twice daily on days 1-21. Glutamine: Administered orally twice daily for 21 days
- analyzed count
- 24
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00365768-om-0001#groups/OG000
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- outcome key
- om-0001
- arm key
- OG001
- arm label
- Arm II: Placebo
- regimen
- Beginning 1 week after administration of vincristine chemotherapy, patients receive oral placebo twice daily on days 1-21. Placebo: Administered orally twice daily for 21 days
- analyzed count
- 25
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00365768-om-0001#groups/OG001
- harms
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- harm key
- EG000
- source section id
- NCT00365768-ae
- event group key
- EG000
- event group label
- Arm I: Glutamine
- serious affected
- 0
- serious at risk
- 24
- other affected
- 0
- other at risk
- 24
- frequency threshold
- 0
- collection period
- Source null
- event definition
- Source null
- undenominated note
- Source null
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- release id
- clinical-indications-draft-1
- disease state id
- ds-kidney-carcinoma
- nct id
- NCT00365768
- harm key
- EG001
- source section id
- NCT00365768-ae
- event group key
- EG001
- event group label
- Arm II
- serious affected
- 0
- serious at risk
- 25
- other affected
- 0
- other at risk
- 25
- frequency threshold
- 0
- collection period
- Source null
- event definition
- Source null
- undenominated note
- Source null
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- quality of life
- setting source links
Preserved source evidence · Not medical advice
Triangle