Comparison the effect of general anesthesia with Sevofluran, Isoflorane and Propofol in decreasing nausea and vomiting after surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201210035543N8

Enrollment

150

Registered

2012-11-17

Start date

2013-02-19

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

Nausea and vomiting. Nausea and vomiting

Interventions

Intervention 1: Group 1: before induction of general anesthesia, all patients per kilogram of body weight,7cc of ringers saline is infusion. 0.5 mg Atracurim and 1.5 µ/gr fentanyl used for induction o

Treatment - Drugs

Group 1: before induction of general anesthesia, all patients per kilogram of body weight,7cc of ringers saline is infusion. 0.5 mg Atracurim and 1.5 µ/gr fentanyl used for induction of anesthesia in

Group2: before induction of general anesthesia, all patients per kilogram of body weight,7cc of ringers saline is infusion. 0.5 mg Atracurim and 1.5 µ/gr fentanyl used for induction of anesthesia in a

Group3: before induction of general anesthesia, all patients per kilogram of body weight,7cc of ringers saline is infusion. 0.5 mg Atracurim and 1.5 µ/gr fentanyl used for induction of anesthesia in a

Eligibility

Sex/Gender

All

Age

50 Years to 70 Years

Inclusion criteria

Inclusion criteria: Exclusion criteria :history of nausea and vomiting after general anesthesia; history of motion sickness;severe hypoxia during anesthesia prolonged anesthesia; using ketamine drugs atvmydat;ranitidine ;metoclopramide ;severe anxiety and severe obesity. Also, due to interference with the metabolism of isoflurane;Phenobarbital;phenytoin; ethanol and isoniazed.non-using of these drugs as well as other condition are considered for the study. Inclusion criteria, all patients 50 to 70 years admitted for cataract surgery to kamkar hospital.

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

Measure	Time frame
Blood pressure. Timepoint: Recovery 3 and 6 hour after surgery. Method of measurement: Monitoring.	—

Primary

Measure	Time frame
Nausea and vomiting. Timepoint: Recovery 3 hour and 6 hour after surgery. Method of measurement: Visual and questions.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mohammad Hossein Pishvaey

Qom University of Medical Science

mkoohbor68@yahoo.com+251 2923957

Outcome results

None listed

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