NCT05061095 · ADVERSE EVENTS

Adverse events

Understanding What Matters Most to Patients: Establishing the Validity of a Best-Worst Scaling Survey · Source last updated 2024-12-27

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.

Collection time frame: Not available. The protocol does not require adverse event assessment.
Other-event reporting threshold: 0%

The protocol does not require adverse event assessment. Adverse Event data was not collected.

Participants affected / participants at risk, as reported
Safety group	Serious events	Other events	Deaths
All Participants Participants who consented to participate and started to study.	0 / 0	0 / 0	0 / 0

Group identifiers: EG000: All Participants

Serious adverse events

Event terms and counts are source-reported; expand to read more. A reporting threshold may omit less frequent events.

Other reported adverse events

Event terms and counts are source-reported; expand to read more. A reporting threshold may omit less frequent events.

Complete source fields

description

The protocol does not require adverse event assessment. Adverse Event data was not collected.

event Groups

deaths Num Affected
0
deaths Num At Risk
0
description
Participants who consented to participate and started to study.
id
EG000
other Num Affected
0
other Num At Risk
0
serious Num Affected
0
serious Num At Risk
0
title
All Participants

frequency Threshold

time Frame

Not available. The protocol does not require adverse event assessment.

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice