Serious Event

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Serious Event

Serious Adverse Events (SAEs) are adverse events that result in death, are life-threatening, require or prolong hospitalization, cause persistent or significant disability/incapacity, or are congenital anomalies/birth defects. Each serious event is categorized by term, organ system, assessment type, and source vocabulary to provide standardized reporting across clinical trials.

Serious Event path is as follows:

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

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

Serious Event

Ignite Creation Date: 2025-12-24 @ 6:33 PM
Ignite Modification Date: 2025-12-25 @ 4:03 PM
NCT ID: NCT01297257
Term: Clinically-driven Target Lesion Revascularization
Organ System: Surgical and medical procedures
Assessment Type: None
Source Vocabulary: None
Notes: Revascularization at target lesion (TL) with positive functional ischemia study/ischemic symptoms AND angiographic minimal lumen diameter stenosis \>=50%, or revascularization of TL with diameter stenosis \>=70% without angina/positive functional study
Study: NCT01297257
Study Brief: DELIVER Study: DELiverability of the Resolute Integrity Stent in All-Comer Vessels and Cross-OvER Stenting
Serious Event Stats (If Any):

Serious Event Stats

Group ID # Events # Affected # At Risk View
EG000 10 10 7740 View