WHO ICTRP trial
Multicenter randomized controlled study of ursodeoxycholic acid on biliary…
ChiCTR-IOR-17011782 · Chinese Clinical Trial Registry (ChiCTR) · Recruiting
Key facts
| Trial ID | ChiCTR-IOR-17011782 |
|---|---|
| Public title | Multicenter randomized controlled study of ursodeoxycholic acid on biliary components and biliary plastic stent permeability |
| Scientific title | Multicenter randomized controlled study of ursodeoxycholic acid on biliary components and biliary plastic stent permeability |
| Primary sponsor | Department of Gastroenterology, The First Affiliated Hospital of Anhui Medical University |
| Registry | Chinese Clinical Trial Registry (ChiCTR) |
| Recruitment status | Recruiting |
| Study type | Interventional study |
| Phase | Other |
| Countries | China |
| Conditions | biliary stricture |
| Interventions | Ursodeoxycholic acid:Ursodeoxycholic acid 13-15mg/kg, 1-2 times daily, treatment time is given for more than12 moths;The control group:Do not give anything |
| Registration date | Jun 28, 2017 |
| Target size | Ursodeoxycholic acid:500;The control group:500 |
| Registry page | chictr.org.cn |
At a glance
- No Results available
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About WHO ICTRP trial registrations
The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.
Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: