Post op Pain in Hip Surgeries
Conditions
Keywords
post op pain in hip surgeries
Brief summary
Lumbar Erector Spinae Plane Block Versus Fascia Iliaca Plane Block in Hip Surgeries as Postoperative Analgesia The aim of this study is to compare the analgesic efficacy of lumbar ElectroSpine Plane Block and Fascia Iliaca Plane Block in patients undergoing hip surgery under spinal anesthesia.
Detailed description
Lumbar Erector Spinae Plane Block Versus Fascia Iliaca Plane Block in Hip Surgeries as Postoperative Analgesia The aim of this study is to compare the analgesic efficacy of lumbar ElectroSpine Plane Block and Fascia Iliaca Plane Block in patients undergoing hip surgery under spinal anesthesia. Primary outcome: • Follow up postoprative pain. Secondary outcome: • Requirment of analgesic drugs either (opoid or non opoid) postoprative.
Interventions
Lumbar Erector Spinae Plane Block Versus Fascia Iliaca Plane Block in Hip Surgeries as Postoperative Analgesia
Sponsors
Sohag University
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Masking description
triple
Intervention model description
compare fascia iliaca plane block versus lumbar Erectospinae plane block in hip replacement as Postoperative Analgesia arm 1 fascia iliaca plane block arm 2 lumber electrospine plane block A standardized analgesic regimen will be prescribed in the postoperative period. Patients will be observed at 0, 2, 4, 6, 12,18 and 24 hours for postoperative VAS scores. All patients will receive paracetamol 1 gm every 6 h as routine analgesia. If VAS is more than 3 intravenous morphine 3mg will be administered as rescue analgesia
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes
Inclusion criteria
* • Age between ≥ 18 years * Both sexes. * American Society of Anesthesiologists (ASA) Physical Status I-III * Undergoing elective unilateral hip surgeries under spinal anesthesia * Patients with body mass index (BMI) \< 35 kg/m²
Exclusion criteria
* • Patient refusal * Known allergy to local anesthetics * Infection at the site of block * Coagulopathy or bleeding disorders * Cognitive impairment affecting pain assessment * Chronic opioid use * Neuromuscular disorders as patients with stroke.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| follow up postoperative pain by Visual Analogue Scale (VAS)score | follow up postoperative pain in 24 hours | follow up postoperative pain every 2hours |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Requirment of analgesic drugs either (opoid or non opoid) postoprative by Viscual Analogue Scale (VAS) Score | Requirment of analgesic drugs either (opoid or non opoid) postoprative. in 24hours | Requirment of analgesic drugs either (opoid or non opoid) postoprative.every 2hours |
Countries
Egypt
Contacts
CONTACThadeer ali, resident
Outcome results
None listed