Health Condition 1: M97- Periprosthetic fracture around internal prosthetic joint
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients presenting for proximal femur fracture surgery (intertrochanteric, neck of femur and subtrochanteric fractures) and consenting for the trial will be included.
Exclusion criteria
Exclusion criteria: inability or refusal to sign informed consent, younger than 50 years, BMI greater than 35 kg/m2, intolerance to any of the drugs used in the study, a history of hepatic or renal insufficiency, coagulopathy, using chronic analgesic drugs; having additional illnesses, including liver or kidney diseases, neurological deficits in the lower extremities and illnesses that interfered with communication skills such as dementia or mechanical ventilation requirement
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total TramadolTimepoint: Total Tramadol consumption in first 24 hours after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| NRS scores during resting and movementTimepoint: at 0, 2, 4, 12 and 24 hrs postop;Opioid-related complications and motor weakness after blockTimepoint: 0, 2, 4, 12 and 24 hrs postop;Patient satisfaction (NRS score 0-10; 0-very unsatisfied and 10-very satisfied)Timepoint: 24 hours after surgery;Time to first analgesic requestTimepoint: 0, 2, 4, 12 and 24 hrs postop | — |
Countries
India
Contacts
Sancheti Hospital