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: 2025-12-25 @ 5:01 AM
Ignite Modification Date: 2025-12-26 @ 4:02 AM
NCT ID: NCT01468818
Description: None
Frequency Threshold: 0
Time Frame: None
Study: NCT01468818
Study Brief: Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Melanoma
Event Groups(If Any):

Event Groups

Title Description Deaths # Affected Deaths # At Risk Serious # Affected Serious # At Risk Other # Affected Other # At Risk View
Immunotherapy for Metastatic Melanoma Patients will receive non-myeloablative lymphodepleting preparative regimen consisting of: Cyclophosphamide: Cyclophosphamide 60 mg/kg/day X 2 days intravenous (IV) in 250 ml dextrose 5% in water (D5W) with Mesna 15 mg/kg/day X 2 days over 1 hr. Fludarabine: Fludarabine 25 mg/m2/day intravenous piggyback (IVPB) daily over 30 minutes for 5 days. Young Tumor Infiltrating Lymphocytes (TIL): Patients will receive non-myeloablative lymphodepleting preparative regimen consisting of cyclophosphamide and fludarabine followed by the administration of young TIL. On day 0, cells (1x10e9 to 2x10e11) will be infused intravenously (i.v.) on the Patient Care Unit over 20 to 30 minutes (between one and four days after the last dose of fludarabine). None None 1 18 18 18 View
Serious Events(If Any):

Serious Events

Term Type Organ System Vocab View
Death not associated with CTCAE term SYSTEMATIC_ASSESSMENT General disorders CTCAE (3.0) View
Infection SYSTEMATIC_ASSESSMENT Infections and infestations CTCAE (3.0) View
AST, SGOT (serum glutamic oxaloacetic transaminase) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Adult Respiratory Distress Syndrome (ARDS) SYSTEMATIC_ASSESSMENT Respiratory, thoracic and mediastinal disorders CTCAE (3.0) View
Other Events(If Any):

Other Events

Term Type Organ System Vocab View
Febrile neutropenia SYSTEMATIC_ASSESSMENT Infections and infestations CTCAE (3.0) View
Allergic reaction/hypersensitivity (including drug fever) SYSTEMATIC_ASSESSMENT Immune system disorders CTCAE (3.0) View
Hemoglobin SYSTEMATIC_ASSESSMENT Blood and lymphatic system disorders CTCAE (3.0) View
Leukocytes (total WBC) SYSTEMATIC_ASSESSMENT Blood and lymphatic system disorders CTCAE (3.0) View
Lymphopenia SYSTEMATIC_ASSESSMENT Blood and lymphatic system disorders CTCAE (3.0) View
Neutrophils/granulocytes (ANC/AGC) SYSTEMATIC_ASSESSMENT Blood and lymphatic system disorders CTCAE (3.0) View
Platelets SYSTEMATIC_ASSESSMENT Blood and lymphatic system disorders CTCAE (3.0) View
Supraventricular and nodal arrhythmia SYSTEMATIC_ASSESSMENT Cardiac disorders CTCAE (3.0) View
Hypotension SYSTEMATIC_ASSESSMENT Cardiac disorders CTCAE (3.0) View
Fever (in the absence of neutropenia, where neutropenia is defined as ANC <1.0x10e9/L) SYSTEMATIC_ASSESSMENT General disorders CTCAE (3.0) View
Rigors/chills SYSTEMATIC_ASSESSMENT General disorders CTCAE (3.0) View
Weight gain SYSTEMATIC_ASSESSMENT General disorders CTCAE (3.0) View
Pruritis/itching SYSTEMATIC_ASSESSMENT Skin and subcutaneous tissue disorders CTCAE (3.0) View
Constipation SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Diarrhea SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Nausea SYSTEMATIC_ASSESSMENT Gastrointestinal disorders CTCAE (3.0) View
Colitis, infectious (e.g., Clostridium difficile) SYSTEMATIC_ASSESSMENT Infections and infestations CTCAE (3.0) View
Infection SYSTEMATIC_ASSESSMENT Infections and infestations CTCAE (3.0) View
ALT/SGPT (serum glutamic pyruvic transaminase) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Albumin, serum-low (hypoalbuminemia) SYSTEMATIC_ASSESSMENT Metabolism and nutrition disorders CTCAE (3.0) View
Alkaline phosphatase 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
Psychosis (hallucinations/delusions) SYSTEMATIC_ASSESSMENT Nervous system disorders CTCAE (3.0) View
Pain SYSTEMATIC_ASSESSMENT General disorders CTCAE (3.0) View
Dyspnea (shortness of breath) SYSTEMATIC_ASSESSMENT Respiratory, thoracic and mediastinal disorders CTCAE (3.0) View
Hypoxia SYSTEMATIC_ASSESSMENT Respiratory, thoracic and mediastinal disorders CTCAE (3.0) View
Incontinence, urinary SYSTEMATIC_ASSESSMENT Renal and urinary disorders CTCAE (3.0) View
Renal/Genitourinary - Other (Oliguria) SYSTEMATIC_ASSESSMENT Renal and urinary disorders CTCAE (3.0) View
Thrombosis/embolism (vascular access-related) SYSTEMATIC_ASSESSMENT Vascular disorders CTCAE (3.0) View
Thrombosis/thrombus/embolism SYSTEMATIC_ASSESSMENT Vascular disorders CTCAE (3.0) View