Pain relief while positioning for Spinal anesthesia and post surgery pain relief following Hip fracture Surgeries

Comparative study of ultrasound guided fascia iliaca compartment block versus pericapsular nerve group block to facilitate positioning for spinal anesthesia and post operative analgesia in hip fracture surgeries - NILL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/06/054465

Enrollment

Registered

2023-06-27

Start date

Unknown

Completion date

Unknown

Last updated

2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Z478- Encounter for other orthopedic aftercare

Interventions

Intervention1: Comparative study of ultrasound guided Fascia Iliaca compartment block with inj 0.2% Ropivacaine 40 ml(one time) ,80 mg dosage and duration of 15 mins: Comparative study of ultrasound g

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients belonging to ASA class I,II and III 2)Patient who has given informed consent 3)Patients undergoing elective hip fracture surgeries under spinal anesthesia 4)weight:-BMI

Exclusion criteria

Exclusion criteria: 1)Patients with hepatic, heart , endocrine and renal diseases 2)Patients with history of coagulopathy 3)patients with infection at site of block 4)Patients with neuropsychiatric disorders 5)Patients refusal 6)Patients with multiple drug allergies 7)All emergency surgical procedures 8)All pregnant and lactating females 9)Patients with inability to comprehend VAS scores

Design outcomes

Primary

Measure	Time frame
1)Pain scores at rest and during 15 degrees passive limb lifting before giving the block and 30mins after giving the block 2)To assess the ease for positioning the patient for spinal anesthesia after performing the block 3)To measure VAS and NRS scores over 24 hours postoperative periodTimepoint: Immediately,30 mins,2hour,6hour,8hour,10 and 12 hours after injection	—

Secondary

Measure	Time frame
-TO MEASURE AMOUNT SYSTEMIC OPIOID USED (NUMBER OF RESCUE DOSES) -PATIENT SATISFACTION AND BLOCK RELATED COMPLICATIONSTimepoint: 2HR,6HR,8HR,10HR,12HR,24HRS AFTER PERFORMING THE BLOCK	—

Countries

India

Contacts

Public ContactDR SMITA DYAVAIAH PATIL

smit271981p@gmail.com9980509370

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026