Health Condition 1: M170- Bilateral primary osteoarthritis of knee Health Condition 2: M19- Other and unspecified osteoarthritis
Conditions
Interventions
Intervention1: Prewarmed intravenous fluid at 40 Degree given in intervention
and fluid at 20 degree Celsius to comparator group.: Group one will be given intravenous fluid at room temperature(20 Degr
Sponsors
NIL
Eligibility
Inclusion criteria
Inclusion criteria: All gender consenting patients undergoing hip or knee arthroplasty surgeries
Exclusion criteria
Exclusion criteria: Patients who will have baseline core body temperature more than 38 or less than 36 Degree Celsius. Patients with impacted wax, perforation of the tympanic membrane, middle/ external ear infections. Those with urinary tract infections, diabetic autonomic neuropathy or any neurological diseases. Patients with deranged coagulation profile. Those with history of allergy to the local anesthetic
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effect of prewarmed intravenous fluid and intravenous fluid at room temperature on core body temperature(tympanic membrane temperature measured by ear thermometer) and shivering, when given to patient during the arthroplasty surgical procedure.Timepoint: Primary outcomes will be assessed at start of surgery, at everyone minute for first 5 minutes, at every 30 mins till completion of surgery(2.5-3.5 hours) in both the groups. In recovery room we will assess the outcome at 0min(when patient reach in recovery room),30min,60min 90min and 120min. | — |
Secondary
| Measure | Time frame |
|---|---|
| To determine the effect of prewarmed intravenous fluid on patient s hemodynamic profile, VAS Score, incidence of nausea vomiting & time to discharge the patient from recovery room. To identify any specific untoward side effects/ complications due to infusion of prewarmed intravenous fluid.Timepoint: Secondary outcomes will be assessed at start of surgery, at everyone minute for first 5 minutes, at every 30 mins till completion of surgery(2.5-3.5 hours) in both the groups. In recovery room we will assess the outcome at 0min(when patient reach in recovery room),30min,60min 90min & 120min. | — |
Countries
India
Contacts
Public ContactDr Mridul Madhav Panditrao
Adesh University, Bathinda
Outcome results
None listed