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Preemptive Analgesic Effects of Popliteal Sciatic Nerve Block in Patients With Bilateral Hallux Valgus Surgery

Prospective, Randomized, Single Blind Trial of Preemptive Analgesic Effects of Popliteal Sciatic Nerve Block in Patients With Bilateral Hallux Valgus Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03414593
Enrollment
20
Registered
2018-01-30
Start date
2018-01-02
Completion date
2018-12-31
Last updated
2018-01-30

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

Conditions

Acute Pain, Pain, Postoperative, Preemptive Peripheral Nerve Block

Keywords

preemptive analgic effect, popliteal sciatic nerve block, Bilateral Hallux Valgus

Brief summary

The purpose of this study was to investigate the preemptive effect of ultrasound guided popliteal scistic nerve block on postoperative acute pain in patients with bilateral hallux valgus. After induction of general anesthesia, the leg to be operated first is decided randomly. After the operation of one leg is completed, PSNB is performed on both legs with 0.2% Ropivacaine and surgery is started on the remaining legs. When the surgery is over, check to see which foot pain begins first, how strong the pain is, and whether there are any side effects.

Interventions

DRUGUltrasound guided popliteal sciatic nerve block with 0.2% ropivcaine

Ultrasound guided popliteal sciatic nerve block with 0.2% ropivacaine 20ml

Sponsors

Asan Medical Center
Lead SponsorOTHER

Study design

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

Intervention model description

Patients who underwent surgery on both feet at the same time. One foot is performed before surgery and the other is performed after surgery.

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. adults between the ages of 20 and 80 2. bilateral hallux valgus surgery on the same day 3. ASA class 1 or 2 4. Patients who have voluntarily agreed in writing to participate in the trial

Exclusion criteria

1. Patient with side effects on local anesthetics or steroids 2. Patient who are taboo of peripheral nerve block such as blood clotting disorder, infection, etc. 3. Patients with uncontrolled medical or psychiatric problem 4. Patient does not agree to participate in the study 5. Patients who are pregnant or lactating

Design outcomes

Primary

MeasureTime frameDescription
Analgesic duration of nerve blockat 0, 0.5, 1, 4, 8, 12 hours after operation. And AM 9 and PM 5 of POD (Post Operative Day) 1The difference of NRS during study time between group preB and group postB The Numeric Rating Scale (NRS-11) is an 11-point scale for patient self-reporting of pain. It is for adults and children 10 years old or older. 0: No pain, 1-3: mild pain, 4-6: Moderate pain, 7-10: severe pain, 10: worst pain imaginable.

Secondary

MeasureTime frameDescription
Difference of analgesic consumption between both groupat 0, 0.5, 1, 4, 8, 12 hours after operation. And AM 9 and PM 5 of POD (Post Operative Day) 1The difference of usage of rescue analgesics during study time between group preB and group postB after the operation
side effect of popliteal sciatic nerve blockat 0, 0.5, 1, 4, 8, 12 hours after operation. And AM 9 and PM 5 of POD (Post Operative Day) 1any other sensation except pain

Countries

South Korea

Outcome results

None listed

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