Bone fracture. Fracture of bone following insertion of orthopedic implant, joint prosthesis, or bone plate
Conditions
Interventions
Intervention 1: Intervention group 1: will receive 0.2 mg of oral clonidine after entering the emergency room. Intervention 2: Control group: They will receive placebo pills from the person responsibl
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients over 18 years old with bone fractures, and pain score >5 based on VASS History of opioid drug abuse Consent to participate in the study
Exclusion criteria
Exclusion criteria: Pregnancy and breastfeeding women History of underlying cardio-pulmonary, renal diseases high blood pressure Thrombocytopenia Asthma Use of narcotics other than morphine The patient's urgent need for blood transfusion or resuscitation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Before the intervention and 30 minutes, 1 hour, 3 hours and 6 hours after the intervention. Method of measurement: Visual pain intensity measurement scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hemodynamic symptoms (systolic and diastolic blood pressure, heart rate, arterial blood oxygen saturation). Timepoint: Before the intervention and 30 minutes, 1 hour, 3 hours and 6 hours after the intervention. Method of measurement: Monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Rostamipour
Kerman University of Medical Sciences
Outcome results
None listed