Clinical trial
A Tolerability and Efficacy Study of TU-100 For The Treatment of Postoperative…
NCT00266461 · Tsumura USA, Industry · Completed
Key facts
| NCT number | NCT00266461 |
|---|---|
| Title | A Tolerability and Efficacy Study of TU-100 For The Treatment of Postoperative Ileus |
| Official title | A Randomized, Controlled, Open-Label Tolerability And Efficacy Study Of TU-100 For The Treatment Of Postoperative Ileus In Patients Undergoing Laparotomy For Large Bowel Resection |
| Lead sponsor | Tsumura USA, Industry |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Postoperative Ileus |
| Intervention type | Drug |
| Interventions | Daikenchuto Extract Granules (TU-100) |
| Enrollment | 24 |
| Start date | Dec 1, 2005 |
| Primary completion | Jan 1, 2008 |
| Completion | Jan 1, 2008 |
| First posted | Dec 16, 2005 |
| Last update posted | Jul 12, 2013 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: