Relation between elective laparoscopic cholecystectomy pain Propofol injection in patients candidate for and Granisetron.
Conditions
Interventions
Intervention 1: Control group (30 hands) which receive normal saline before Propofol injection. Intervention 2: Intervention group (30 hands) which receive Granisetron before Propofol injection.
Placebo
Prevention
Control group (30 hands) which receive normal saline before Propofol injection.
Intervention group (30 hands) which receive Granisetron before Propofol injection.
Sponsors
Tehran University of Medical Sciences and Health Services
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Ages between 20 and 50; ASA class 1, 2; Candidate for elective laparoscopic cholecystectomy Exclusion criteria: Past medical history of neurological disease; Chronic pain syndrome; Thrombophlebitis; Advanced systemic disease such as advanced diabetes; Any vascular disease; Any contraindication for Granisetron or Propofol injection
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity. Timepoint: During injection. Method of measurement: Numeric Rating Scale mentioned by the patient. | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative Nausea and Vomiting. Timepoint: In the recovery room. Method of measurement: Nausea and vomiting expressed by the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Ali Movafegh
Tehran University of Medical Sciences, Anesthesiology Department
Outcome results
None listed