Trial Outcomes & Findings for RICE Trial: Rifaximin In Chronic Hepatic Encephalopathy - A Randomized, Controlled Trial (NCT NCT00364689)
NCT ID: NCT00364689
Last Updated: 2019-09-17
Results Overview
TERMINATED
PHASE3
13 participants
Month 7
2019-09-17
Participant Flow
The number of participants that were assigned to each Arm/Group is not known due to the data for this study no longer being available as the retention period has passed.
Participant milestones
| Measure |
All Participants
|
|---|---|
|
Overall Study
STARTED
|
13
|
|
Overall Study
COMPLETED
|
12
|
|
Overall Study
NOT COMPLETED
|
1
|
Reasons for withdrawal
| Measure |
All Participants
|
|---|---|
|
Overall Study
Lost to Follow-up
|
1
|
Baseline Characteristics
RICE Trial: Rifaximin In Chronic Hepatic Encephalopathy - A Randomized, Controlled Trial
Baseline characteristics by cohort
Baseline data not reported
PRIMARY outcome
Timeframe: Month 7Population: Outcome measure data is not reported as the study was terminated due to difficulty with enrolling participants. Collection of data ceased and data analysis was not performed. Data collected is no longer available as the retention period has passed.
Outcome measures
Outcome data not reported
PRIMARY outcome
Timeframe: Month 7Population: Outcome measure data is not reported as the study was terminated due to difficulty with enrolling participants. Collection of data ceased and data analysis was not performed. Data collected is no longer available as the retention period has passed.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Month 7Population: Outcome measure data is not reported as the study was terminated due to difficulty with enrolling participants. Collection of data ceased and data analysis was not performed. Data collected is no longer available as the retention period has passed.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Month 7Population: Outcome measure data is not reported as the study was terminated due to difficulty with enrolling participants. Collection of data ceased and data analysis was not performed. Data collected is no longer available as the retention period has passed.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Month 7Population: Outcome measure data is not reported as the study was terminated due to difficulty with enrolling participants. Collection of data ceased and data analysis was not performed. Data collected is no longer available as the retention period has passed.
Outcome measures
Outcome data not reported
Adverse Events
All Study Participants
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place