Post operative pain. Complex regional pain syndrome I of unspecified lower limb
Conditions
Interventions
Intervention 1: Intervention group: The study group will be received dexmedetomidine 1 micg/kg of body weight for dexamethasone. Intervention 2: Control group: will be received 25 milliliter isotonic
Treatment - Drugs
Placebo
Intervention group: The study group will be received dexmedetomidine 1 micg/kg of body weight for dexamethasone
Control group: will be received 25 milliliter isotonic saline
Sponsors
Oroumia University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patient with class I to III America society of Anesthesiologists; surgery with spinal anesthesia
Exclusion criteria
Exclusion criteria: Cardiovascular disease; Neuropathic Disease; Congenital deformity in the treated organ; Sensitivity to drugs used in the study; Arthroplasty for revision
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain. Timepoint: In recovery, 6 and 12 hours after surgery. Method of measurement: Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| The average need for an analgesic drug to control pain. Timepoint: In 12 hours after surgery. Method of measurement: milligram.;The first time to apply for post-operative pain control. Timepoint: In 12 hours after surgery. Method of measurement: hour.;Postoperative bleeding is to 12 hours. Timepoint: In 12 hours after surgery. Method of measurement: Based on the amount of blood in the Hamovak donor, it is determined in 24 hours and the amount of hemoglobin in the postoperative patients.;Sleep disorder after surgery. Timepoint: In 24hours after surgery. Method of measurement: Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShahryar Sane
Oroumia University of Medical Sciences
Outcome results
None listed