Trial Outcomes & Findings for A Comparison of Mometasone to Advair in Patients With Milder Persistent Asthma (NCT NCT00461812)

NCT ID: NCT00461812

Last Updated: 2017-09-20

Results Overview

Recruitment status

TERMINATED

Study phase

PHASE4

Target enrollment

33 participants

Primary outcome timeframe

change from baseline to study completion

Results posted on

2017-09-20

Participant Flow

33 participants were consented for this study. However, there were 23 pre-randomization screening failures. Only 10 were enrolled. The number of participants assigned/randomized to each Arm/Group is unknown.

Participant milestones

Participant milestones
Measure
All Participants
Mometasone or Advair
Overall Study
STARTED
10
Overall Study
COMPLETED
0
Overall Study
NOT COMPLETED
10

Reasons for withdrawal

Reasons for withdrawal
Measure
All Participants
Mometasone or Advair
Overall Study
study terminated
10

Baseline Characteristics

A Comparison of Mometasone to Advair in Patients With Milder Persistent Asthma

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
All Participants
n=10 Participants
Mometasone or Advair
Age, Customized
>=18, <=16 years
10 Participants
n=5 Participants
Sex: Female, Male
Female
6 Participants
n=5 Participants
Sex: Female, Male
Male
4 Participants
n=5 Participants
Region of Enrollment
United States
10 participants
n=5 Participants

PRIMARY outcome

Timeframe: change from baseline to study completion

Population: There is no data available for this outcome measure. The study was prematurely terminated and the PI is no longer with the institution. The information available was obtained from the IRB.

Outcome measures

Outcome data not reported

Adverse Events

All Participants

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Johns Hopkins University Clinical Trials Program

Johns Hopkins University School of Medicine

Phone: 410-550-6484

Results disclosure agreements

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