NCT02176083 · ADVERSE EVENTS

Adverse events

Reproductive Health Survivorship Care Plan Pilot · Source last updated 2020-04-20

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 reported
Other-event reporting threshold: 0%

Participants affected / participants at risk, as reported
Safety group	Serious events	Other events	Deaths
Intervention Text message management prompts: YBCS will receive text message prompts on how to manage hot flashes and vaginal dryness Text message management prompts	0 / 11	0 / 11	Not reported / Not reported
Control Control YBCS will not receive text message prompts on managing hot flashes and vaginal dryness	0 / 27	0 / 27	Not reported / Not reported

Group identifiers: EG000: Intervention · EG001: Control

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

event Groups

description
Text message management prompts: YBCS will receive text message prompts on how to manage hot flashes and vaginal dryness Text message management prompts
id
EG000
other Num Affected
0
other Num At Risk
11
serious Num Affected
0
serious Num At Risk
11
title
Intervention
description
Control YBCS will not receive text message prompts on managing hot flashes and vaginal dryness
id
EG001
other Num Affected
0
other Num At Risk
27
serious Num Affected
0
serious Num At Risk
27
title
Control

frequency Threshold

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

Preserved source evidence · Not medical advice