Post-procedural Pain. Other acute postprocedural pain
Conditions
Interventions
Intervention 1: Intervention group: Clonidine produced by Zahravi Tabriz Company will be given orally to the patients in the form of 0.2 mg tablet twice daily. Intervention 2: Control group: Placebo p
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Age of 18 to 70 years Weight 60 to 80 kg Having satisfaction Adherence of clinical signs and symptoms to MRI findings The presence of a disc in a lumbar space in an MRI
Exclusion criteria
Exclusion criteria: History of lumbar surgery Drug or Alcohol Addiction Pregnancy and lactation Previous use of the same drugs Seizures and other neurological diseases Intervention over a diskette only involves the use of a discectomy or diskette over a disk space Use of other medications the day before or after surgery (unwanted) The patient's disability is due to retardation, aphasia, visual impairment, and other things that prevent the patient from communicating. The patient's over-standard need for opioid and analgesic neuropathic drugs History of obstructive peripheral vascular disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-operative pain. Timepoint: Clonidine used in capsule form and 2 hours before surgical intervention in the case group will be given to patients. After surgery for the first 24 hours and at the end of 6 hours, one physician who is blind to the study will record the parametric / VAS pain rate in the sheet. The amount of Opioid ingestion in the first 24 hours after surgery will also be measured for each patient. Method of measurement: Using VAS (virtual analogue scale) to measure pain in the lower extremities and wrists of patients receiving clonidine and placebo. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactJavad Aghazade
Tabriz University of Medical Sciences
Outcome results
None listed