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Supraclavicular Blocks for Post-Operative Pain Control in Supracondylar Fracture Fixation, a Retrospective Analysis of Single Shot Catheter Techniques

Ann & Robert H Lurie Children's Hospital of Chicago logo

Ann & Robert H Lurie Children's Hospital of Chicago

Status

Unknown

Conditions

Pain, Postoperative
Acute Pain

Treatments

Procedure: Elbow Fracture Fixation

Study type

Interventional

Funder types

Other

Identifiers

NCT02210429
2014-15849

Details and patient eligibility

About

We hypothesize that patients who receive a supraclavicular block via Angiocath, placed intra-operatively and dosed post-operatively following neurologic examination, will have lower pain scores, lower use of intravenous morphine equivalents in the post-anesthesia care unit, and lower rates of intervention for post-operative nausea and vomiting. We also hypothesize that patients receiving this nerve block had the same rates of nerve damage as the patients who did not receive a block and that there will be no demonstrable safety concerns with this block.

Enrollment

200 estimated patients

Sex

All

Ages

Under 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age under 18
  • Undergoing supracondylar fracture fixation in operating room

Exclusion criteria

  • Incomplete or inaccessable chart data

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

200 participants in 4 patient groups

IV Opioids
Active Comparator group
Treatment:
Procedure: Elbow Fracture Fixation
Supraclavicular Single-Shot Block
Active Comparator group
Treatment:
Procedure: Elbow Fracture Fixation
Supraclavicular Catheter
Active Comparator group
Treatment:
Procedure: Elbow Fracture Fixation
Supraclavicular Angiocath
Active Comparator group
Treatment:
Procedure: Elbow Fracture Fixation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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