WHO ICTRP trial
Randomized evaluative study of phenylephrine or norepinephrine for maintenance…
ChiCTR-IIR-16008596 · Chinese Clinical Trial Registry (ChiCTR) · Not Recruiting
Key facts
| Trial ID | ChiCTR-IIR-16008596 |
|---|---|
| Public title | Randomized evaluative study of phenylephrine or norepinephrine for maintenance of blood pressure during spinal anaesthesia for caesarean delivery: The RESPOND3 study |
| Scientific title | Randomized evaluative study of phenylephrine or norepinephrine for maintenance of blood pressure during spinal anaesthesia for caesarean delivery: The RESPOND3 study |
| Primary sponsor | The Chinese University of Hong Kong |
| Registry | Chinese Clinical Trial Registry (ChiCTR) |
| Recruitment status | Not Recruiting |
| Study type | Interventional study |
| Phase | IV (Phase IV study) |
| Countries | China |
| Conditions | Hypotension |
| Interventions | Two groups:Norepinephrine versus phenylephrine, Intravenous infusion. Norepinephrine 7.5 mcg/ml, Approx 30 min; phenylephrine 100 mcg/ml Approx 30 min |
| Registration date | Jun 3, 2016 |
| Target size | Two groups:274 |
| Secondary IDs | CUHK_CCRB00514 |
| Registry page | chictr.org.cn |
At a glance
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: