Trial Outcomes & Findings for Rapid HIV Testing Program in the Emergency Department (NCT NCT00548041)
NCT ID: NCT00548041
Last Updated: 2015-11-02
Results Overview
Feasibility was assessed as number of participants who were approached and agreed to participate in rapid HIV testing and then had testing completed.
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
100 participants
Primary outcome timeframe
2 years
Results posted on
2015-11-02
Participant Flow
Participant milestones
| Measure |
Subjects Undergoing Rapid HIV Testing in the ED
Subjects were seen in the ED and had rapid HIV testing performed.
|
|---|---|
|
Overall Study
STARTED
|
100
|
|
Overall Study
COMPLETED
|
100
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Rapid HIV Testing Program in the Emergency Department
Baseline characteristics by cohort
| Measure |
Subjects Undergoing Rapid HIV Testing in the ED
n=100 Participants
Subjects were seen in the ED and had rapid HIV testing performed.
|
|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=5 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
97 Participants
n=5 Participants
|
|
Age, Categorical
>=65 years
|
3 Participants
n=5 Participants
|
|
Sex: Female, Male
Female
|
64 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
36 Participants
n=5 Participants
|
|
Region of Enrollment
United States
|
100 participants
n=5 Participants
|
PRIMARY outcome
Timeframe: 2 yearsFeasibility was assessed as number of participants who were approached and agreed to participate in rapid HIV testing and then had testing completed.
Outcome measures
| Measure |
Subjects Undergoing Rapid HIV Testing in the ED
n=100 Participants
Subjects were seen in the ED and had rapid HIV testing performed.
|
|---|---|
|
Feasibility of Rapid HIV Testing in Emergency Department
|
100 participants
|
Adverse Events
Subjects Undergoing HIV Testing in the ED
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
| Measure |
Subjects Undergoing HIV Testing in the ED
|
|---|---|
|
Blood and lymphatic system disorders
Adverse Events were not collected/addressed
|
—
0/0
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place