WHO ICTRP trial
A 8 week, Randomized, Double-blind, Placebo-Controlled Clinical Trial for the…
KCT0008170 · Clinical Research Information Service (CRIS) · Not Recruiting
Key facts
| Trial ID | KCT0008170 |
|---|---|
| Public title | A 8 week, Randomized, Double-blind, Placebo-Controlled Clinical Trial for the Evaluation of the Efficacy and Safety of OFE on Memory Improvement of Adolescent |
| Scientific title | A 8 week, Randomized, Double-blind, Placebo-Controlled Clinical Trial for the Evaluation of the Efficacy and Safety of OFE on Memory Improvement of Adolescent |
| Primary sponsor | Konkuk University Medical Center |
| Registry | Clinical Research Information Service (CRIS) |
| Recruitment status | Not Recruiting |
| Study type | Interventional Study |
| Phase | Not applicable |
| Countries | Korea, Republic of |
| Conditions | Not Applicable |
| Interventions | Dietary Supplement : Take 3 tablets of test food (1,920 mg/day as extract from Opuntia ficus-indica) or placebo(850mg/capsule) once a day with water. |
| Registration date | Feb 10, 2023 |
| Target size | 56 |
| Registry page | cris.nih.go.kr |
At a glance
- No Results available
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: