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

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

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 years

Feasibility was assessed as number of participants who were approached and agreed to participate in rapid HIV testing and then had testing completed.

Outcome measures

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

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

Dr. Ellen Tedaldi

Temple University Hospital

Phone: 215-707-2000

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place