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To compare Ultrasound-Guided Nerve Block and Combined Foot and Ankle Nerve Block for pain relief after foot surgery

A comparative study to evaluate the effectiveness of ultrasound-guided popliteal nerve block and a combination of ultrasound guided interfacial plane foot block with sural nerve block on postoperative analgesia in patients undergoing calcaneal surgery. A Randomized Controlied Trial. - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073817
Enrollment
60
Registered
2024-09-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: M97-M97- Periprosthetic fracture around internal prosthetic joint

Interventions

Intervention1: Group-1 Ultrasound-guided Popliteal Nerve Block : patients will be randomly allocated to receive Popliteal nerve block with 10 ml of local anesthetic (LA). The block will be give once

Sponsors

Sancheti Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults of either gender aged between age between 18- and 80-years with American Society of Anesthesiologists (ASA) physical status I to III undergoing calcaneal surgery

Exclusion criteria

Exclusion criteria: 1. Patients with coagulopathy, sepsis, hepatic or renal failure 2. allergy to local anesthetic (LA) 3.Inability to consent to the study 4. Patients having opioids previously 5. Patients with pre-existing neuropathies 6. Patients with local infection around the needle site

Design outcomes

Primary

MeasureTime frame
The times of rescue analgesia and the adverse reactions caused by the analgesics such as pruritus, nausea and vomiting will be recorded. Timepoint: time to anlgesia requirement when patient demandsin first 24 hours

Secondary

MeasureTime frame
1.The visual assessment scale (VAS) was used to assess the pain of patients immediately after discharge from the operating room (T1), at 1st (T2), 2nd (T3), 4th (T4), 8th (T5),2th (T6), and 24th (T7) hour after operation. 2.The satisfaction of the surgeon and patients the satisfaction concerning the block received on a Likert scale of 1-5 ( 1: least likely and 5: most likely) 3.Total tramadol consumption in 24 hours Timepoint: VAS will be recorded at time 0, 1 h, 2 h,4h, 8h, 12 h and 24 h total tramadol will be recorded once at 24 h

Countries

India

Contacts

Public ContactDr Sandeep Diwan

Sancheti Institute for Orthopedics and Rehabiliation

sdiwan1965@gmx.com9823029328

Outcome results

None listed

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