WHO ICTRP trial
Comparison study of the pre emptive of the two dose of dexmedetomidine (bolus…
IRCT20101211005362N31 · Iranian Registry of Clinical Trials (IRCT) · Recruiting
Key facts
| Trial ID | IRCT20101211005362N31 |
|---|---|
| Public title | Comparison study of the pre emptive of the two dose of dexmedetomidine (bolus and infusion) on post operative pain, nausea and vomiting for laparoscopic cholecystectomy |
| Scientific title | Comparison study of the preemptive of the two dose of dexmedetomidine (bolus and infusion) on post operative pain, nausea and vomiting for laparoscopic cholecystectomy |
| Primary sponsor | Esfahan University of Medical Sciences |
| Registry | Iranian Registry of Clinical Trials (IRCT) |
| Recruitment status | Recruiting |
| Study type | interventional |
| Phase | 1-2 |
| Countries | Iran (Islamic Republic of) |
| Conditions | Pain, nausea and vomiting. |
| Interventions | Intervention 1: Intervention group: Intravenous dexmedetomidine at a dose of 1 microgram per kilogram of body weight is given as a bolus dose 20 minutes before induction of anesthesia and then 0.5 micrograms per kilogram of body weight for… |
| Registration date | Nov 7, 2022 |
| Target size | 90 |
| Registry page | irct.behdasht.gov.ir |
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: