Health Condition 1: M169- Osteoarthritis of hip, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who will require unilateral total hip replacement and are willing to give consent to take part in the study will be included.
Exclusion criteria
Exclusion criteria: Patients who refuse to give their consent Age less than 18 Years ASA 4 or above Local anesthetic allergy Local sepsis or infection at puncture site Patients with bleeding diathesis Patients with peripheral neuropathy Patients with dementia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numerical Pain Rating ScaleTimepoint: Every 12 hourly till 96 Hours | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objective is to assess 1.Time To First Rescue Analgesic(TTRFA) 2.Number of rescue analgesia consumed 3.Time to ambulate 4.Length of hospital stay 5.Incidence of complicationsTimepoint: Every 12 hourly | — |
Countries
India
Contacts
Christian Medical College, Vellore