Bone Cement Implantation Syndrome.
Conditions
Interventions
Intervention 1: Intervention group: One venous infusion of one 100 mg/2 ml ampoule of ABURAIHAN Co. hydrocortisone during the cement implantation. Intervention 2: Control group: No venous injection of
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age over 18 years Need for Arthroplasty Willingness to participate in the study
Exclusion criteria
Exclusion criteria: History of dementia or psychiatric and psychological disorders that affect decision-making power
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of patients with high heart Rate. Timepoint: Before anesthesia, before implanting cement, immediately after implanting cement, and half an hour after implanting cement. Method of measurement: Heart Monitoring.;Percentage of patients with blood pressure drop. Timepoint: Before anesthesia, before implanting cement, immediately after implanting cement, and half an hour after implanting cement. Method of measurement: Sphygmomanometer.;Percentage of patients with oxygen saturation drop. Timepoint: Before anesthesia, before implanting cement, immediately after implanting cement, and half an hour after implanting cement. Method of measurement: Pulse Oxymeter.;PCO2. Timepoint: half an hour after implanting cement. Method of measurement: Arterial Blood Gas. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAli Yeganeh
Iran University of Medical Sciences
Outcome results
None listed