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Lateral upper thigh approach to sciatic and femoral nerve blocks in children

Lateral supratrochanteric approach to sciatic and femoral nerve blocks in children: a feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN70969666
Enrollment
20
Registered
2017-09-20
Start date
2017-01-09
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

Lower extremity surgery Surgery

Interventions

Single shot neurostimulator-guided sciatic and femoral nerve blocks with bupivacaine 0.25% 0.3 ml/kg and 0.3 ml/kg respectively. All participants received sciatic and femoral neve blocks in the opera

Sponsors

Lviv Regional Childrens' Clinic Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. 5-18 year old children of both genders undergoing lower limb surgery below middle of thigh 2. ASA status 1 or 2 3. Parental written informed consent for SNB, FNB and study participation

Exclusion criteria

Exclusion criteria: 1. Anatomical abnormality in block region 2. Contraindications to regional anesthesia

Design outcomes

Primary

MeasureTime frame
1. The possibility of single injection site sciatic and femoral nerve blocks: 1.1. The possibility to perform sciatic nerve block from supratrochanteric area along mid-axillary line was assessed once at the moment of performing the block and was defined as possibility of eliciting motor response (plantar flexion) on neurostimulation with following neurostimulator settings: current 0.4 mA, impulse duration 0.3 ms and impulse frequency 2 Hz 1.2. The possibility to perform femoral nerve block from the same point also was assessed once at the moment of performing the block and was defined as possibility of eliciting motor response (patellar twitches) on neurostimulation with the same settings

Secondary

MeasureTime frame
1. Skin to nerve distances assessed once at the moment of performing the blocks using insulated needles with centimeter markings (Stimuplex A, 21G, 150 mm, B.Braun, Melsungen, Germany). The depth of needle insertion equaled to skin-to-corresponding nerve distance. 2. Pain intensity assessed according to Numeric Rating Scale (NRS, 0-10 points) during the first postoperative day at 1, 3, 6, 12 and 24 postoperative hours

Countries

Ukraine

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 27, 2026