WHO ICTRP trial
Efficacy and safety of intravenous acetaminophen for postoperative…
ChiCTR2100054865 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting
Key facts
| Trial ID | ChiCTR2100054865 |
|---|---|
| Public title | Efficacy and safety of intravenous acetaminophen for postoperative morphine-assisted analgesia: a two-stage multicenter, randomized, double-blind, placebo-controlled parallel clinical trial (Stage II) |
| Scientific title | Efficacy and safety of intravenous acetaminophen for postoperative morphine-assisted analgesia: a two-stage multicenter, randomized, double-blind, placebo-controlled parallel clinical trial (Stage II) |
| Primary sponsor | West China Hospital, Sichuan University |
| Registry | Chinese Clinical Trial Registry (ChiCTR) |
| Recruitment status | Not Recruiting |
| Study type | Interventional study |
| Phase | 4 |
| Countries | China |
| Conditions | orthopedic surgery |
| Interventions | Intravenous acetaminophen group:500 mg intravenous acetaminophen every 6 h for 24 h;Placebo group:the same volume of saline every 6 h for 24 h |
| Registration date | Dec 28, 2021 |
| Target size | Intravenous acetaminophen group:120;Placebo group:120 |
| Registry page | chictr.org.cn |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: