Adverse Events Module

Adverse Events Module

For researchers submitting trial data to ClinicalTrials.gov, the Adverse Events module is one of four mandatory results sections. It requires reporting in three primary categories: All-Cause Mortality: A table tracking all deaths that occurred during the study, regardless of cause. Serious Adverse Events (SAEs): A tabular summary of events resulting in death, life-threatening conditions, hospitalization, or significant disability. Other Adverse Events: A table for non-serious events that exceed a specific frequency threshold, such as 5% within any study arm.

Adverse Events Module path is as follows:

Study -> Results Section -> Adverse Events Module -> Event Groups

Study -> Results Section -> Adverse Events Module -> Serious Events

Study -> Results Section -> Adverse Events Module -> Other Events

Adverse Events Module


Ignite Creation Date: 2025-12-24 @ 2:53 PM
Ignite Modification Date: 2025-12-25 @ 1:19 PM
NCT ID: NCT00335959
Description: None
Frequency Threshold: 5
Time Frame: Patients were assessed for adverse events after pre-operative chemotherapy, after pre-operative chemoradiation and within 14 days of surgery.
Study: NCT00335959
Study Brief: S0425 Oxaliplatin, Capecitabine, and RT in Treating Patients W/Stomach Cancer That Can Be Removed By Surgery
Event Groups(If Any):

Event Groups

Title Description Deaths # Affected Deaths # At Risk Serious # Affected Serious # At Risk Other # Affected Other # At Risk View
Chemotherapy, Chemoradiation and Surgery Patients were to receive Oxaliplatin 130 mg/m2 (2 hour IV infusion on Days 1 and 22), Capecitabine 850 mg/m2/dose (PO q 12 hours on Days 1-14 and 22-35), Capecitabine 650 mg/m2/dose (PO q 12 hours on days 43-77), Radiation therapy 180 cGy/day, 5 days/week beginning on Day 43. Patients with stable disease or better were to have distal subtotal gastrectomy, total gastrectomy, or proximal gastrectomy. None None 1 6 6 6 View
Serious Events(If Any):

Serious Events

Term Type Organ System Vocab View
Gastrointestinal-Other (Specify) SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Other Events(If Any):

Other Events

Term Type Organ System Vocab View
Diarrhea SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Hemoglobin SYSTEMATIC_ASSESSMENT Blood and lymphatic system disorders CTCAE (3.0) View
Ventricular arrhythmia - PVCs SYSTEMATIC_ASSESSMENT Cardiac disorders CTCAE (3.0) View
Constipation SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Dysphagia (difficulty swallowing) SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Heartburn/dyspepsia SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Mucositis/stomatitis (clinical exam) - Oral cavity SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Mucositis/stomatitis (functional/symptomatic) - Oral cavity SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Necrosis, GI - Small bowel NOS SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Pain - Abdomen NOS SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Pain - Esophagus SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Pain - Intestine SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Pain - Stomach SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Fatigue (asthenia, lethargy, malaise) SYSTEMATIC_ASSESSMENT General disorders CTCAE (3.0) View
Infection (documented clinically or microbiologically) with Grade 3 or 4 neutrophils - Urinary tract SYSTEMATIC_ASSESSMENT Infections and infestations CTCAE (3.0) View
ALT, SGPT (serum glutamic pyruvic transaminase) SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
AST, SGOT (serum glutamic oxaloacetic transaminase) SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
Alkaline phosphatase SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
Neutrophils/granulocytes (ANC/AGC) SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
Platelets SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
Weight loss SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
Albumin, serum-low (hypoalbuminemia) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Anorexia SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Calcium, serum-high (hypercalcemia) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Calcium, serum-low (hypocalcemia) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Dehydration SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Glucose, serum-high (hyperglycemia) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Phosphate, serum-low (hypophosphatemia) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Potassium, serum-low (hypokalemia) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Sodium, serum-low (hyponatremia) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Pain - Joint SYSTEMATIC_ASSESSMENT Musculoskeletal and connective tissue disorders CTCAE (3.0) View
Neuropathy: sensory SYSTEMATIC_ASSESSMENT Nervous system disorders CTCAE (3.0) View
Mood alteration - anxiety SYSTEMATIC_ASSESSMENT Psychiatric disorders CTCAE (3.0) View
Dry skin SYSTEMATIC_ASSESSMENT Skin and subcutaneous tissue disorders CTCAE (3.0) View
Photosensitivity SYSTEMATIC_ASSESSMENT Skin and subcutaneous tissue disorders CTCAE (3.0) View
Rash: hand-foot skin reaction SYSTEMATIC_ASSESSMENT Skin and subcutaneous tissue disorders CTCAE (3.0) View
Nausea SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Vomiting SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Creatinine SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
Leukocytes (total WBC) SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
Lymphopenia SYSTEMATIC_ASSESSMENT Investigations CTCAE (3.0) View
Hypotension SYSTEMATIC_ASSESSMENT Vascular disorders CTCAE (3.0) View