The effect of Granisetron on pain of Propofol injectio
Not Applicable
- Conditions
- Relation between elective laparoscopic cholecystectomy pain Propofol injection in patients candidate for and Granisetron.
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
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
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity. Timepoint: During injection. Method of measurement: Numeric Rating Scale mentioned by the patient.
- Secondary Outcome Measures
Name Time Method Postoperative Nausea and Vomiting. Timepoint: In the recovery room. Method of measurement: Nausea and vomiting expressed by the patient.