Comparison of combination of two classes of adjuvants on duration of analgesia and visual analogue scores for postoperative analgesia in proximal femoral nailing surgeries

Ultrasound guided suprainguinal fascia iliaca compartment block for proximal femoral nailing surgeries under spinal anaesthesia Comparison of efficacy of combination of dexamethasone and dexmedetomidine as adjuvants versus dexamethasone alone with ropivacaine - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/069438

Enrollment

120

Registered

2024-06-25

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: S720- Fracture of head and neck of femur Health Condition 2: S720- Fracture of head and neck of femur Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Suprainguinal fascia iliaca compartment block: Ultrasound guided suprainguinal fascia iliaca compartment block immediately after spinal anaesthesia Patient then Monitored for 24hours p

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists (ASA) physical status I or II, who were scheduled for proximal femoral nailing (PFN) surgery (for Inter-trochanteric fracture femur) by surgeons with identical surgical expertise, under subarachnoid block were registered in this trail.

Exclusion criteria

Exclusion criteria: patients with coagulation abnormalities, cerebrovascular diseases, cognitive impairment, poly-trauma, hepatic and renal failure,subjects having local site infection or altered anatomy like inguinal hernia, allergy to study drugs, and pregnancy were excluded from the study.

Design outcomes

Primary

Measure	Time frame
Duration of postoperative analgesiaTimepoint: First 24 hours of postoperative period	—

Secondary

Measure	Time frame
Quality of block Haemodynamic variations Level of sedation Adverse effectsTimepoint: First 24 hours of postoperative period	—

Countries

India

Contacts

Public ContactK Sree lekha

Government Medical College Kadapa

s.durga.dr@gmail.com9177923023

Outcome results

None listed

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