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comparison of popliteal and parasacral ischial plane block

Comparison Of efficacy of Ultrasound Guided Parasacral Ischial Plane (PIP) Block Versus Popliteal Sciatic Nerve Block for Below Knee Surgeries: A Randomized Non-Inferiority Trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062409
Enrollment
50
Registered
2024-02-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Ultrasound Guided Parasacral Ischial Plane (PIP) Block for Below Knee Surgeries using Bupivacaine 0.5%: - Efficacy of ultrasound guided parasacral ischial plane block - single shot of 0

Sponsors

Jawaharlal Institute of Postgraduate Medical College and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients of either gender, between 18-70 years of age, un-dergoing below knee surgeries will be included in this trial.

Exclusion criteria

Exclusion criteria: 1) History of allergy to local anesthetics, 2) Patient with coagulopathies or on anticoagulant therapy 3) Infection at the injection site 4) Patients who are pre operatively on opioids 5) Patients planned for surgery under tourniquet 6) Patient with hemodynamic instability and significant car-diovascular disease

Design outcomes

Primary

MeasureTime frame
1)To evaluate the efficacy of Ultrasound guided Parasacral Ischial Plane (PIP )block over Poplite-al sciatic nerve approach for below knee surger-ies( i.e., Onset of sensory and motor blockade in minutes )Timepoint: Onset of sensory and motor block will be assessed every 1 minute till sensory and motor is achieved

Secondary

MeasureTime frame
1) Total duration for performance of block 2) Duration of analgesia 3) Comparison of intra-operative opioid use be-tween the groups 4) Ease of block performance 5) Complications during the procedure 6) Patient satisfaction score Timepoint: Vas scores, duration of analgesia, patient satifsaction score will be assessed at baseline, 4 hours, 8 hours, 12hours & 24 hours.

Countries

India

Contacts

Public ContactDr Santhosh A

Jawaharlal Institute of Postgraduate Medical Education and Research

jipmersrinivasan@gmail.com9626493045

Outcome results

None listed

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