Skip to content

comparison of ultrasound guided lower thigh versus mid thigh local anaesthetic injections for post-operative pain relief for surgeries in and around knee

ultrasound guided 4 in 1 block versus adductor canal block for post-operative analgesia for surgeries in and around knee-a comparative study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/040900
Enrollment
60
Registered
2022-03-08
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: M170- Bilateral primary osteoarthritis of knee Health Condition 2: S870- Crushing injury of knee Health Condition 3: M232- Derangement of meniscus due to oldtear or injury Health Condition 4: S820- Fracture of patella Health Condition 5: S821- Fracture of upper end of tibia Health Condition 6: S810- Open wound of knee Health Condition 7: M179- Osteoarthritis of knee, unspecified Health Condition 8: M220- Recurrent dislocation of patella Health Condition 9: S834- Sprain of col

Interventions

Intervention1: four in one block or adductor cannal block: Either four in one block or adductor cannal block using 0.25% bupivacaine local anaesthetic for post operative pain relief VAS score given af

Sponsors

Navodaya medical college hospital and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex 2. Patients in the age group of 18-60 years 3. Patients of ASA physical Status I & II 4.Patients who are oriented to give consent 5. Patients undergoing elective surgeries in and around knee under sub arachnoid block

Exclusion criteria

Exclusion criteria: 1. Patientâ??s refusal for the procedure 2. Patients with significant coagulopathies and other contra-indications for regional anaesthesia. 3. Patients with pre-existing significant systemic diseases. 4. Patients with psychiatric history. 5. Patient allergic to amide local anesthetics. 6. Infection of the skin at the injection site.

Design outcomes

Primary

MeasureTime frame
1. Visual Analogue Score less than 3 Timepoint: 1. Post operative VAS score at 0hr, 2hrs, 6hrs, 8hrs 12hrs and 24hrs.

Secondary

MeasureTime frame
Time duration since block for first dose of rescue opioid.Timepoint: In hours

Countries

India

Contacts

Public ContactNikhil M

Navodaya Medical college hospital and research centre

drvishalakshi_patil@yahoo.co.in9986901256

Outcome results

None listed

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