Trial Outcomes & Findings for Risperidone Treatment in Schizophrenia Patients Who Are Currently Taking Clozapine (NCT NCT00056498)
NCT ID: NCT00056498
Last Updated: 2019-10-01
Results Overview
The Brief Psychiatric Rating Scale (BPRS) positive symptom items are: conceptual disorganization, hallucinatory behavior, unusual thought content, and suspiciousness. The total score is calculated by adding the scores for each item. Each scale ranges from "1=Not Present" to "7=Very Severe". The minimum score is 4 and the maximum score is 28. A higher score indicates a more severe positive symptom rating. A mixed model for unbalanced repeated measures analysis of covariance (ANCOVA), in which follow-up symptom score = baseline symptom score + treatment + week + treatment x week, and week is treated as a categorical, rather than a continuous measure. The treatment term estimates the average across weeks of the week-specific group differences, and is used as the main test for treatment effects on symptom change.
COMPLETED
PHASE4
65 participants
Baseline and every two weeks for 16 weeks.
2019-10-01
Participant Flow
Though funding was in place beginning in 2001, recruitment took place from 2003 to 2008. Subjects were recruited from the Maryland Psychiatric Research Center Outpatient Reseach clinic, the Treatment Research Program, and community mental health centers.
86 Participants signed informed consent. 15 were ineligible or excluded. 71 Participants entered the evaluation phase. Two were withdrawn prior to randomization. Four people withdrew after randomization but prior to starting study medications.
Participant milestones
| Measure |
Risperidone
Participants assigned to risperidone
|
Placebo
Participants assigned to placebo
|
|---|---|---|
|
Overall Study
STARTED
|
30
|
35
|
|
Overall Study
COMPLETED
|
25
|
28
|
|
Overall Study
NOT COMPLETED
|
5
|
7
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Risperidone Treatment in Schizophrenia Patients Who Are Currently Taking Clozapine
Baseline characteristics by cohort
| Measure |
Risperidone
n=30 Participants
Participants assigned to risperidone
|
Placebo
n=35 Participants
Participants assigned to placebo
|
Total
n=65 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
30 Participants
n=99 Participants
|
35 Participants
n=107 Participants
|
65 Participants
n=206 Participants
|
|
Age, Categorical
>=65 years
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Age, Continuous
|
48.3 years
STANDARD_DEVIATION 7.2 • n=99 Participants
|
44.1 years
STANDARD_DEVIATION 9.3 • n=107 Participants
|
46.1 years
STANDARD_DEVIATION 8.6 • n=206 Participants
|
|
Sex: Female, Male
Female
|
11 Participants
n=99 Participants
|
10 Participants
n=107 Participants
|
21 Participants
n=206 Participants
|
|
Sex: Female, Male
Male
|
19 Participants
n=99 Participants
|
25 Participants
n=107 Participants
|
44 Participants
n=206 Participants
|
|
Region of Enrollment
United States
|
30 participants
n=99 Participants
|
35 participants
n=107 Participants
|
65.0 participants
n=206 Participants
|
PRIMARY outcome
Timeframe: Baseline and every two weeks for 16 weeks.Population: The intent to treat analysis included all participants who received at least one dose of study medication and completed the BPRS rating at the specified week.
The Brief Psychiatric Rating Scale (BPRS) positive symptom items are: conceptual disorganization, hallucinatory behavior, unusual thought content, and suspiciousness. The total score is calculated by adding the scores for each item. Each scale ranges from "1=Not Present" to "7=Very Severe". The minimum score is 4 and the maximum score is 28. A higher score indicates a more severe positive symptom rating. A mixed model for unbalanced repeated measures analysis of covariance (ANCOVA), in which follow-up symptom score = baseline symptom score + treatment + week + treatment x week, and week is treated as a categorical, rather than a continuous measure. The treatment term estimates the average across weeks of the week-specific group differences, and is used as the main test for treatment effects on symptom change.
Outcome measures
| Measure |
Risperidone
n=30 Participants
Participants assigned to risperidone
|
Placebo
n=34 Participants
Participants assigned to placebo
|
|---|---|---|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 10
|
13.9 units on a scale
Standard Deviation 4.2
|
14.9 units on a scale
Standard Deviation 4.2
|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 12
|
13.8 units on a scale
Standard Deviation 3.7
|
15.3 units on a scale
Standard Deviation 4.6
|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 14
|
13.4 units on a scale
Standard Deviation 3.5
|
14.2 units on a scale
Standard Deviation 3.8
|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 16
|
13.2 units on a scale
Standard Deviation 3.5
|
14.1 units on a scale
Standard Deviation 3.6
|
|
Positive Symptom Item Scores by Week and Treatment Group
Change Score
|
-2.6 units on a scale
Standard Deviation 3.1
|
-1.5 units on a scale
Standard Deviation 3.4
|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 0
|
15.5 units on a scale
Standard Deviation 3.8
|
15.5 units on a scale
Standard Deviation 4.2
|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 2
|
14.6 units on a scale
Standard Deviation 3.7
|
15.1 units on a scale
Standard Deviation 4.0
|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 4
|
13.3 units on a scale
Standard Deviation 4.0
|
14.4 units on a scale
Standard Deviation 3.5
|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 6
|
13.9 units on a scale
Standard Deviation 3.9
|
14.7 units on a scale
Standard Deviation 3.8
|
|
Positive Symptom Item Scores by Week and Treatment Group
Week 8
|
13.5 units on a scale
Standard Deviation 4.2
|
14.9 units on a scale
Standard Deviation 3.9
|
SECONDARY outcome
Timeframe: Baseline and Week 16Population: Two participants completed 9 or fewer of the 13 individual tests in the neurocognitive battery, and were omitted from calculation of the overall composite score
The neuropsychological testing measured attention, executive function/problem solving, motor speed, processing speed/response generation, and verbal, visual, and working memory. The individual test raw scores were converted to z-scores and an overall composite z-score was computed from the average of the individual test z-scores. Z-scores range from -3 standard deviations up to +3 standard deviations. Higher scores indicate better test performance.
Outcome measures
| Measure |
Risperidone
n=24 Participants
Participants assigned to risperidone
|
Placebo
n=27 Participants
Participants assigned to placebo
|
|---|---|---|
|
Neuropsychological Testing - Overall Composite Z-score
Baseline
|
0.02 z-score
Standard Deviation 0.66
|
-0.03 z-score
Standard Deviation 0.46
|
|
Neuropsychological Testing - Overall Composite Z-score
Week 16
|
0.12 z-score
Standard Deviation 0.66
|
0.07 z-score
Standard Deviation 0.47
|
SECONDARY outcome
Timeframe: Baseline and every two weeks for 16 weeks.Population: The intent to treat analysis included all participants who received at least one dose of study medication and completed the SANS rating at the specified treatment week.
The Scale for the Assessment of Negative Symptoms (SANS) total score, minus the global items, inappropriate affect, poverty of content of speech, and attention items, used to measure negative symptoms. SANS total score range = 0-85. Higher scores indicate more severe negative symptoms. A mixed model for unbalanced repeated measures analysis of covariance (ANCOVA), in which follow-up symptom score = baseline symptom score + treatment + week + treatment x week, and week is treated as a categorical, rather than a continuous measure. The treatment term estimates the average across weeks of the week-specific group differences, and is used as the main test for treatment effects on symptom change.
Outcome measures
| Measure |
Risperidone
n=30 Participants
Participants assigned to risperidone
|
Placebo
n=34 Participants
Participants assigned to placebo
|
|---|---|---|
|
Negative Symptom Total Score by Week and Treatment Group
Week 0
|
32.3 units on a scale
Standard Deviation 11.6
|
33.0 units on a scale
Standard Deviation 13.3
|
|
Negative Symptom Total Score by Week and Treatment Group
Week 2
|
30.8 units on a scale
Standard Deviation 11.5
|
34.0 units on a scale
Standard Deviation 12.1
|
|
Negative Symptom Total Score by Week and Treatment Group
Week 4
|
29.8 units on a scale
Standard Deviation 11.6
|
32.9 units on a scale
Standard Deviation 13.3
|
|
Negative Symptom Total Score by Week and Treatment Group
Week 6
|
31.2 units on a scale
Standard Deviation 10.3
|
33.0 units on a scale
Standard Deviation 12.7
|
|
Negative Symptom Total Score by Week and Treatment Group
Week 8
|
30.4 units on a scale
Standard Deviation 11.3
|
34.0 units on a scale
Standard Deviation 14.1
|
|
Negative Symptom Total Score by Week and Treatment Group
Week 10
|
30.6 units on a scale
Standard Deviation 10.9
|
33.1 units on a scale
Standard Deviation 13.3
|
|
Negative Symptom Total Score by Week and Treatment Group
Week 12
|
31.6 units on a scale
Standard Deviation 10.7
|
32.4 units on a scale
Standard Deviation 12.5
|
|
Negative Symptom Total Score by Week and Treatment Group
Week 14
|
31.7 units on a scale
Standard Deviation 11.0
|
34.4 units on a scale
Standard Deviation 14.1
|
|
Negative Symptom Total Score by Week and Treatment Group
Week 16
|
31.3 units on a scale
Standard Deviation 11.9
|
34.4 units on a scale
Standard Deviation 14.8
|
|
Negative Symptom Total Score by Week and Treatment Group
Change Score
|
-2.6 units on a scale
Standard Deviation 5.6
|
1.1 units on a scale
Standard Deviation 10.8
|
Adverse Events
Risperidone
Placebo
Serious adverse events
| Measure |
Risperidone
n=30 participants at risk
Participants assigned to risperidone
|
Placebo
n=35 participants at risk
Participants assigned to placebo
|
|---|---|---|
|
Psychiatric disorders
increased auditory hallucinations
|
3.3%
1/30
|
0.00%
0/35
|
|
Gastrointestinal disorders
gastrointestinal symptoms
|
0.00%
0/30
|
2.9%
1/35
|
|
Psychiatric disorders
Panic attack
|
0.00%
0/30
|
2.9%
1/35
|
Other adverse events
Adverse event data not reported
Additional Information
Robert W. Buchanan, MD
Maryland Psychiatric Research Center
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place