WHO ICTRP trial
Patient controlled analgesia i.v. with morphine versus continuous epidural…
NL-OMON44865 · Overview of Medical Research in the Netherlands (NL-OMON) · Not Recruiting
Key facts
| Trial ID | NL-OMON44865 |
|---|---|
| Public title | Patient controlled analgesia i.v. with morphine versus continuous epidural analgesia with bupivacaïne and sufentanil as pain relief after caesarean section. |
| Scientific title | Patient controlled analgesia i.v. with morphine versus continuous epidural analgesia with bupivacaïne and sufentanil as pain relief after caesarean section. - GAstudy |
| Primary sponsor | Kennemer Gasthuis |
| Registry | Overview of Medical Research in the Netherlands (NL-OMON) |
| Recruitment status | Not Recruiting |
| Study type | Interventional |
| Countries | The Netherlands |
| Conditions | pain relief after caesarean section;10036411;10029903;pain relief after caesarean section |
| Interventions | Group A will get iv PCA with morphine 2mg/ml, bolus 2 mg, lock out period 5 minutes, with a maximum of 30 mg in 4 hours. Group B will get continuous epidural analgesia (CEA) with bupivacaine 0,125% (50 ml) combined with sufentanil 50… |
| Registration date | Apr 10, 2018 |
| Target size | 70 |
| Secondary IDs | 2013-00-5168-25;NL45365.094.13 |
| Registry page | onderzoekmetmensen.nl |
At a glance
- No Results available
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: