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Popliteal Block for Lower Limb Angioplasty

The Benefit of Popliteal Sciatic Nerve Block for Lower Limb Angioplasty in Critical Limb Ischemia: a Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04445480
Enrollment
40
Registered
2020-06-24
Start date
2019-05-07
Completion date
2020-03-01
Last updated
2020-06-24

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

Conditions

Anaesthesia and Analgesia, Angioplasty

Keywords

popliteal block, chronic limb ischemia

Brief summary

Endovascular revascularization is an effective procedure in treatment of chronic critical limb ischemia. The less invasive procedure in high risk patients produce the benefit to the patients. However, some of the patients cannot tolerate local anaesthesia. These patients need sedation or even general anaesthesia, which increase unnecessary risk to the patients. This study is conducted to evaluate the benefit of popliteal sciatic nerve block or popliteal block compare to sedation in critical limb patients undergoing angioplasty.

Interventions

Sciatic nerve block at popliteal fossa would perform before the participant undergoing angioplasty in experimental arm.

OTHERControl

Sciatic nerve at popliteal fossa would be scanned with the ultrasound. The toothpick would be applied to simulate the procedure of nerve block.

Sponsors

Mahidol University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age more than 20 year-old with chronic ischemic limb pain * Scheduled for peripheral angioplasty under monitor anaesthesia care * Expected timing of procedure not more than 3 hours

Exclusion criteria

* Age less than 21 * Cannot cooperate with the staff * Having pain in other areas or both legs * Contraindicate for nerve block * Allergy to local anesthetic drugs or sedative drugs

Design outcomes

Primary

MeasureTime frame
Incidence of general anaesthesiaFive hours

Secondary

MeasureTime frame
Numerical pain rating scale during procedureFive hours

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026