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A Novel Selective Block of the Suprascapular Nerve

A Novel Selective Block of the Suprascapular Nerve

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02035774
Enrollment
30
Registered
2014-01-14
Start date
2014-01-31
Completion date
2014-06-30
Last updated
2014-06-17

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

Conditions

Fracture, Ligament Injury

Keywords

Brachial plexus block, Suprascapular nerve block

Brief summary

Patients who receive the lateral and sagittal infraclavicular block (LSIB) tend to supinate their hand and forearm which may hamper optimal positioning for surgery of the dorsal side of the hand. The investigators think that this supination is caused by lateral rotation in the shoulder. The main lateral rotator of the shoulder is the infraspinatus muscle, which is innervated by the suprascapular nerve (SSN).The investigators hypothesized that optimal positioning of the hand for surgery on the dorsal side of the hand may be achieved by performing a SSN block (SSNB) in addition to the LSIB.

Detailed description

According to the hypothesis the investigators will perform a double blind , placebo controlled study to answer the research question above.

Interventions

PROCEDURELSIB + SSNB

Patients will receive LSIB (31 ml ropivacaine 7.5 mg/ml)+ SSNB (4 ml Ropivacaine 5 mg/ml) or LSIB (31 ml ropivacaine 7.5 mg/ml)+ SSNB (4 ml placebo, saline)

Sponsors

University of Tromso
CollaboratorOTHER
University Hospital of North Norway
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients with American Society of Anesthesiologists physical status (ASA) I- III * age between 18 and 70 years * body mass index between 20 and 36 kg/m2 scheduled for elective hand surgery.

Exclusion criteria

We will measure the angle between wrist and horizontal plane while the patient is supine and the extended arm 75° abducted. * Patient who are not able to pronate the hand ≤15° before block performance, will be excluded from the study. * Patients will also be excluded if they are pregnant, have contraindications to regional anesthesia, coagulation disorder, allergy to local anesthetics (LA), atrioventricular block, peripheral neuropathy or drug-treated diabetes. * Patients using other anticoagulation drugs than acetylsalicylic acids or dipyridamol will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Wrist angle30 minutesThe investigators will assess the wrist angle 30 minutes after the two blocks (LSIB + SSNB)

Secondary

MeasureTime frameDescription
Satisfaction score3 hoursThe investigators will ask the surgeons about his/her satisfaction with the hand position during surgery.

Countries

Norway

Outcome results

None listed

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