Trial · NCT00202293
Comparison of Combination Olanzapine+Lithium or Chlorpromazine+Lithium in Treatment of First Manic Episode With Psychotic Features
NCT00202293, Phase 4, Completed, Melbourne Health
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Combination Olanzapine+Lithium or Chlorpromazine+Lithium in Treatment of First Manic Episode With Psychotic Features. Trials, record NCT00202293. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00202293
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of Combination Olanzapine+Lithium or Chlorpromazine+Lithium in Treatment of First Manic Episode With Psychotic Features
- NCT number
- NCT00202293
- Status
- Completed
- Phases
- Phase 4
- Enrollment
- 83 participants, actual
- Lead sponsor
- Melbourne Health
- Conditions
- Bipolar Disorder, Schizoaffective Disorder
- Interventions
- Olanzapine, Lithium, Chlorpromazine
- First posted
- 2005-09-20
- Last updated
- 2018-08-31
Source ClinicalTrials.gov
Registered outcomes23
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Intensity of side effects | 8 weeks | Intensity of side effects |
| Primary | ¨The frequency of treatment-emergent adverse events (events that first appear or worsen during the study period) will be compared between both groups. | 8 weeks | |
| Primary | ¨The frequency of side effects as rated with the UKU scale will be compared between both groups. | 8 weeks | |
| Primary | ¨Weight gain will be compared between both groups. | 8 weeks | |
| Primary | ¨Frequency of changes in vital signs and laboratory findings will be compared between both groups. | 8 weeks | |
| Primary | Subjective well being | 8 weeks | |
| Primary | ¨Total scores on the DAI and the SWN will be compared between both groups. | 8 weeks | |
| Secondary | Adherence | 8 weeks | |
| Secondary | ¨Degree of adherence to the treatment as scored on the MARS will be compared between both groups. | 8 weeks | |
| Secondary | Response to treatment | 8 weeks |
1 to 10 of 23Source ClinicalTrials.gov
See all 23 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00202293
GET https://conductscience.org/api/trials/v1/NCT00202293/registered?page=2