List B in the California Verbal Learning Test (CVLT) score range 1-16; the score is the number of words recalled so higher scores = better performance/more words recalled.
| Group | Value | 95% CI |
|---|---|---|
| Citicoline, Creatine, and Omega-3 Arm | 10 | 1 – 16 |
Last reviewed · How we verify
Citicoline, Creatine, and Omega-3 Effects in Middle Age Women
NA trial testing Citicoline, Omega-3 Fatty Acids and Creatine in Cognitive Benefits in 40 participants. Completed in 1 November 2019.
| Lead sponsor | Deborah Yurgelun-Todd |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 40 |
| Start date | 1 February 2012 |
| Primary completion | 30 October 2018 |
| Estimated completion | 1 November 2019 |
| Sites | 1 location across United States |
Deborah Yurgelun-Todd — full company profile →
Adults 40 to 60, female only, with Cognitive Benefits. Patients with the condition only — healthy volunteers not accepted.
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
List B in the California Verbal Learning Test (CVLT) score range 1-16; the score is the number of words recalled so higher scores = better performance/more words recalled.
| Group | Value | 95% CI |
|---|---|---|
| Citicoline, Creatine, and Omega-3 Arm | 10 | 1 – 16 |
WAIS-IV Block Design Subtest A test of visuoconstructional ability is recognized as a test of visuospatial planning and function. It has been shown to be correlated with measures of general intellectual ability. The score range for this measure is 0-129. A score of 90-110 is average for a standard score. The higher the score the better the outcome.
| Group | Value | 95% CI |
|---|---|---|
| Citicoline, Creatine, and Omega-3 Arm | 98 | 0 – 130 |
The purpose of this study is to determine the functional effects of a citicoline, creatine, and omega-3 fatty acids combination when administered for a duration of four weeks (28 days) to non-psychiatric adult female participants.
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01502813.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing