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Plantar Compartment Block in Hallux Valgus Ambulatory Surgery

Analgesia Quality and Quality of Deambulation of the Plantar Compartment Block After Hallux Valgus Ambulatory Surgery.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03815422
Acronym
Observationnal
Enrollment
30
Registered
2019-01-24
Start date
2017-12-01
Completion date
2019-12-31
Last updated
2020-03-10

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

Conditions

Hallux Valgus Ambulatory Surgery

Keywords

Early ambulation, Plantar block

Brief summary

Hallux valgus surgery is known as a painful surgery. Qualitative pain management is the key to successful early recovery and rehabilitation. Popliteal sciatic nerve block is widely used despite the risk of falling due to prolonged motor blockade. Plantar block combined with distal peroneal block may be a better analgesic option in order to provide fast track rehabilitation. The purpose of this study is to describe the analgesic effect of the plantar compartment block following hallux valgus surgery.

Interventions

PROCEDURERegional anesthesia

Short lasting sciatic nerve block and long lasting plantar block with distal deep peroneal block

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

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

Inclusion criteria

* Age between 18 and 75 years old * patient covered by social health insurance * have signed written informed consent * scheduled for hallux valgus ambulatory surgery

Exclusion criteria

* protected patients or patients incapable of giving written informed consent * pregnant or breastfeeding woman * vulnerable adult * inability to participate in pain scoring scales * severe coagulopathy * allergy or contraindications to study drugs * preopérative gait disorders * chronic kidney disease with glomerular filtration rate (GFR) ≤ 50 ml/min (estimated by the Cockroft and Gault formula) * severe chronic liver disease * chronic pain (treated by non steroidal anti inflammatory drugs, opioids, neuroleptic drugs, antidepressant or anticonvulsants) * peripheral neuropathy * intervention under general anesthesia

Design outcomes

Primary

MeasureTime frameDescription
Analgesia quality of the plantar compartment block48 hoursafter Hallux Valgus ambulatory surgery

Secondary

MeasureTime frameDescription
Quality of deambulationQuality of deambulation during the first 2 postoperative days.48 hours
postoperative analgesicpostoperative analgesic requirement, during the first 2 postoperative days.48 hours

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026