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Effect of Ondansetron, Metoclopramide and Dexamethasone on Post Operative Nausea Vomiting after strabismus surgery

Effect of Ondansetron, Metoclopramide and Dexamethasone on Post Operative Nausea Vomiting after strabismus surgery

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201012051138N4
Enrollment
111
Registered
2011-01-05
Start date
2007-11-04
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

strabismus. H50

Interventions

Intervention 1: Group A (ondansetron) 0.1mg/kg IV 30 minutes before ending surgery. Intervention 2: Group B ( metoclopramide) 0.15mg/kg IV 30 minutes before ending surgery. Intervention 3:
Treatment - Drugs
Group A (ondansetron) 0.1mg/kg IV 30 minutes before ending surgery
Group B ( metoclopramide) 0.15mg/kg IV 30 minutes before ending surgery
Group C ( dexamethasone) 0.15mg/kg IV at the start of surgery

Sponsors

Guilan University of Medical Sciences,Vice Chancellor for Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 15 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- The patients candidates for strabismus surgery between 2-15 years 2- physical class status(ASA) I-II Exclusion criteria: 1-Historyof GI problems 2-History of known drug sensitivity to drugs used in study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Frequency of nausea and vomiting. Timepoint: In the first hour (recovery period) 1to 6 , 6 to 12 , 12to24 hours post – operation. Method of measurement: Questionnair.

Secondary

MeasureTime frame
Frequency of nausea and vomiting treatment. Timepoint: In the first hour (recovery period) 1to 6 , 6 to 12 , 12to24 hours post – operation. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sudabeh Haddadi

Guilan University of Medical Sciences

So_haddadi@gums.ac.ir+98 13 1222 5242

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026