MedPath

Ultrasound Guided Block For Below Knee Surgeries

Not yet recruiting
Conditions
Diseases of the musculoskeletal system and connective tissue,
Registration Number
CTRI/2020/11/029117
Lead Sponsor
Vinayaka Missions Medical College
Brief Summary

Spinal anaesthesia remains as an established technique for lower limb surgeries, but it has its own adverse effects in perioperative morbidity. With a good knowledge of dermatomes, myotomes and osteotomes of lower limbs and the use of ultrasound for peri-neural deposition of local anaesthetics, we can  overcome the adverse effects of spinal anaesthesia. Neuraxial blocks can be catastrophic due to instability of haemodynamic parameters and coagulopathy. To overcome the adverse effects of other modes of anaesthesia, studies shows, ultrasound guided peripheral nerve blocks can be a safe alternative.

This study aims to delineate the sensory and motor block onset time, hemodynamic parameters and duration of post-operative analgesia for below – knee surgery under ultrasound guided combined popliteal sciatic and adductor canal block.

200 patients of either sex coming for elective below knee surgeries will be this study .Patients allergic to local anaesthetic agents, opiods, patients with Neurological deficits, patients not willing or non-co-operative for the procedure are excluded from this study.

After obtaining consent ,ultrasound guided popliteal sciatic and adductor canal block will be given.

The degree of motor and sensory  blockade ,hemodynamic parameters, ease of positioning ,patient comfort will be noted.

Post operatively, time required for ambulation and time requirement for the need of analgesics are noted.

Incidence of complication if any, and comfort of the surgeon will aso be noted

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

1.ASA 1, ASA 2,ASA 3,ASA 4 2.In-Patient undergoing below knee surgeries.

Exclusion Criteria

1.Patients allergic to local anaesthetic agents, opioids 2.Patients with Neurological deficits 3.Patients not willing or non-co-operative for the procedure.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time required to ambulateImmediately after surgery and every 30 minutes there after
Secondary Outcome Measures
NameTimeMethod
Degree of motor blockade as judged by modified Bromage scaleImmediately after surgery and every 15 minutes there after
Ease of surgery as determined by the surgeonAfter completion of surgery
Post-operative analgesia durationImmediately after surgery and every 15 minutes there after till administration of analgesics
Patient satisfactionAfter positioning for surgery and end of the surgery

Trial Locations

Locations (1)

Vinayaka Missions Medical College

🇮🇳

Karaikal, PONDICHERRY, India

Vinayaka Missions Medical College
🇮🇳Karaikal, PONDICHERRY, India
Dr K Cheran
Principal investigator
9443144652
anscheran.k73@gmail.com

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