Adverse events94

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

1 to 20 of 94

Type	Event	Organ system	Group	Affected	At risk
other	Fatigue	General disorders	FOLFOX Plus Regorafenib	31	39
other	Anemia	Blood and lymphatic system disorders	FOLFOX Plus Regorafenib	28	39
other	White blood cell decreased	Investigations	FOLFOX Plus Regorafenib	28	39
other	Peripheral sensory neuropathy	Nervous system disorders	FOLFOX Plus Regorafenib	27	39
other	Platelet count decreased	Investigations	FOLFOX Plus Regorafenib	27	39
other	Hypertension	Vascular disorders	FOLFOX Plus Regorafenib	25	39
other	Nausea	Gastrointestinal disorders	FOLFOX Plus Regorafenib	23	39
other	Neutrophil count decreased	Investigations	FOLFOX Plus Regorafenib	23	39
other	Alanine aminotransferase increased	Investigations	FOLFOX Plus Regorafenib	21	39
other	Aspartate aminotransferase increased	Investigations	FOLFOX Plus Regorafenib	20	39
other	Mucositis oral	Gastrointestinal disorders	FOLFOX Plus Regorafenib	14	39
other	Palmar-plantar erythrodysesthesia syndrome	Skin and subcutaneous tissue disorders	FOLFOX Plus Regorafenib	14	39
other	Alkaline phosphatase increased	Investigations	FOLFOX Plus Regorafenib	13	39
other	Anorexia	Metabolism and nutrition disorders	FOLFOX Plus Regorafenib	12	39
other	Diarrhea	Gastrointestinal disorders	FOLFOX Plus Regorafenib	12	39
other	Constipation	Gastrointestinal disorders	FOLFOX Plus Regorafenib	11	39
other	Dry skin	Skin and subcutaneous tissue disorders	FOLFOX Plus Regorafenib	11	39
other	Vomiting	Gastrointestinal disorders	FOLFOX Plus Regorafenib	10	39
other	Hyperglycemia	Metabolism and nutrition disorders	FOLFOX Plus Regorafenib	9	39
other	Weight loss	Investigations	FOLFOX Plus Regorafenib	9	39

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
ClinicalTrials.govNo license stated
NIH RePORTER's clinical studies and project filesPublic domain

Each source's terms

ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
ClinicalTrials.govnone stated
NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this list from software.

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GET https://conductscience.org/api/trials/v1/NCT01913639/events

API reference For AI assistants

Adverse events94

Sources 3

Read this list from software.