Effect of DA-5515 (Circulan® Soft Cap.) in Patients With Chronic Fatigue Symptoms Due to Impaired Blood Circulation
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| ClinicalTrials.gov Identifier: NCT03542721 |
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Recruitment Status : Unknown
Verified June 2018 by Dong-A Pharmaceutical.
Recruitment status was: Recruiting
First Posted : May 31, 2018
Last Update Posted : June 4, 2018
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Fatigue Symptom | Drug: DA-5515 Drug: Placebo of DA-5515 | Phase 4 |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 204 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | A Placebo-controlled, Randomized, Double-blind, Parallel, Multi-center Clinical Trial to Evaluate the Efficacy and Safety of DA-5515 (Circulan® Soft Cap.) in Patients With Chronic Fatigue Symptoms Due to Impaired Blood Circulation |
| Actual Study Start Date : | January 17, 2018 |
| Estimated Primary Completion Date : | June 2019 |
| Estimated Study Completion Date : | December 2019 |
| Arm | Intervention/treatment |
|---|---|
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Placebo Comparator: Placebo of DA-5515 Capsule
Placebo of DA-5515 (three times a day)
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Drug: Placebo of DA-5515
Placebo (three times a day)
Other Name: Placebo capsule |
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Experimental: DA-5515 Capsule
Garlic oil, Gingko biloba ex.,Crataegus berry ex.,Melissa officinalis ex., (three times a day)
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Drug: DA-5515
Crataegi ethanol extract, Garlic oil, Ginkgo leaf extract, Melissa folium extract (three times a day)
Other Name: Circulan® Soft Capule |
- CIS(Checklist Individual Strength) less than or equal to 76 [ Time Frame: 8weeks ]Rate of subjects whose CIS score has improved less than or equal to 76 at 8weeks
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 19 Years to 79 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Rutherford's category 0/0 or Ⅰ/1
- ABI <1.0
- CIS greater than 76
- HADS less than or equal to 10
- Subjects who have fatigue symptoms more than 1 month
Exclusion Criteria:
- Subjects who have diseases that can cause fatigue
- Subjects who are taking medication that can cause fatigue
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03542721
| Contact: Ran Seo | 010-4547-1480 | seoran@dreamwiz.com | |
| Contact: WhanSeok Choi | 02-2258-6285 | fmchs@catholic.ac.kr |
| Korea, Republic of | |
| Seoul St. Mary's Hospital | Recruiting |
| Seoul, Korea, Republic of | |
| Contact: Ran Seo 010-4547-1480 seoran@dreamwiz.com | |
| Principal Investigator: | WhanSeok Choi | Seoul St. Mary's Hospital |
| Responsible Party: | Dong-A Pharmaceutical |
| ClinicalTrials.gov Identifier: | NCT03542721 |
| Other Study ID Numbers: |
DA-5515 |
| First Posted: | May 31, 2018 Key Record Dates |
| Last Update Posted: | June 4, 2018 |
| Last Verified: | June 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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chronic fatigue symptom blood circulation |
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Fatigue |

