regional anesthesia. Local anaesthetics
Conditions
Interventions
Intervention 1: Group intervention: All patients would receive the same premedication (200 ml of normal saline, 1.5 mg of midazolam and 75 micrograms fentanyl). 200mg of lidocaine diluted with normal
Treatment - Drugs
Group intervention: All patients would receive the same premedication (200 ml of normal saline, 1.5 mg of midazolam and 75 micrograms fentanyl). 200mg of lidocaine diluted with normal saline associate
Group control: All patients would receive the same premedication (200 ml of normal saline, 1.5 mg of midazolam and 75 micrograms fentanyl). In the control group of 20 patients , 200mg of lidocaine dil
Sponsors
Vice chancellor for research,babol University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: 15 to 70-year-old patients with upper extremity surgery with ASA class 1,2 are enrolled. Exclusion criteria: patients with lidocaine allergy, emergency patients, addict and psychological disorders.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative Pain. Timepoint: 1, 6, 12, 24 Hours after operation. Method of measurement: VAS scale pain.;Overall analgesic requirement post operative. Timepoint: in the first 24 hours after operation. Method of measurement: Nursing Report.;Onset sensory block. Timepoint: From the start of anesthetics injection. Method of measurement: Evaluate the patients response to needle hitting on surgical site.;Tourniquet site pain. Timepoint: Tourniquet pain expressed by patients after applying the tourniquet and during surgery. Method of measurement: Visual Analogue Scale (VAS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShahram Seyfi
Babol University of Medical Sciences
Outcome results
None listed