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.

Recruitment status

COMPLETED

Study phase

PHASE4

Target enrollment

65 participants

Primary outcome timeframe

Baseline and every two weeks for 16 weeks.

Results posted on

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 Two were withdrawn prior to randomization.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

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

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

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 16

Population: 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

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

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

Serious events: 1 serious events
Other events: 0 other events
Deaths: 0 deaths

Placebo

Serious events: 2 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

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

Phone: 410-402-7876

Results disclosure agreements

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