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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00918190
Other study ID # RP 0917
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2009
Est. completion date December 2010

Study information

Verified date October 2021
Source King Khaled Eye Specialist Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this trial is to study the effects of different combinations of antiemetics on the incidence of late onset postoperative nausea and vomiting.


Description:

The authors will study the effect of many antiemetics on the occurrence of nausea and vomiting following strabismus surgery in pediatrics.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender All
Age group 4 Years to 12 Years
Eligibility Inclusion Criteria: - children undergoing elective strabismus surgery under general anesthesia Exclusion Criteria: - children experienced retching or vomiting - children who have taken anti-emetic medications, antihistaminics, steroids, or psychoactive drugs within 24 hours before surgery

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Placebo
Saline
Ondansetron, Dexamethasone
Use of ondansetron and dexamethasone as combined antiemetics
Midazolam, dexamethasone
use of midazolam and dexamethasone as combined antiemetic

Locations

Country Name City State
Saudi Arabia king Khaled Eye Specialist hospital Riyadh

Sponsors (1)

Lead Sponsor Collaborator
King Khaled Eye Specialist Hospital

Country where clinical trial is conducted

Saudi Arabia, 

References & Publications (1)

Riad W, Altaf R, Abdulla A, Oudan H. Effect of midazolam, dexamethasone and their combination on the prevention of nausea and vomiting following strabismus repair in children. Eur J Anaesthesiol. 2007 Aug;24(8):697-701. Epub 2007 Apr 17. Erratum in: Eur J Anaesthesiol. 2008 Jan;25(1):88. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy of antiemetics combination 3 days
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