Trials / Completed
CompletedNCT03258229
Efficacy and Safety of Angelica Gigas N. Extract on Improvement of Hyperglycemia
A 8-week, Randomized, Double-blind, Placebo-controlled 2x2 Cross-over Design Human Trial to Evaluate the Efficacy and Safety of Angelica Gigas N. Extract on Improvement of Hyperglycemia
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Chonbuk National University Hospital · Academic / Other
- Sex
- All
- Age
- 20 Years – 80 Years
- Healthy volunteers
- Accepted
Summary
This study was conducted to investigate the effects of daily supplementation of Angelica gigas N. extract on improvement of Hyperglycemia .
Detailed description
This study was a 8 weeks, randomized, double-blind, placebo-controlled 2×2 cross-over design human trial. Twenty subjects were randomly divided into Angelica gigas N. extract or a placebo group. Fasting and postprandial glucose profiles during oral glucose tolerance test (OGTT) were assessed before and after the intervention.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Angelica gigas N. extract | capsules(2cap/d, 1,000mg/d) for 8 weeks. |
| DIETARY_SUPPLEMENT | Placebo | Placebo for 8 weeks |
Timeline
- Start date
- 2017-02-09
- Primary completion
- 2017-12-07
- Completion
- 2017-12-07
- First posted
- 2017-08-23
- Last updated
- 2019-08-22
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03258229. Inclusion in this directory is not an endorsement.