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

NCT ID: NCT02210429

Last Updated: 2015-07-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-01-31

Study Completion Date

2015-11-30

Brief Summary

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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.

Detailed Description

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Conditions

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Acute Pain Pain, Postoperative

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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IV Opioids

Group Type ACTIVE_COMPARATOR

Elbow Fracture Fixation

Intervention Type PROCEDURE

Supraclavicular Single-Shot Block

Group Type ACTIVE_COMPARATOR

Elbow Fracture Fixation

Intervention Type PROCEDURE

Supraclavicular Catheter

Group Type ACTIVE_COMPARATOR

Elbow Fracture Fixation

Intervention Type PROCEDURE

Supraclavicular Angiocath

Group Type ACTIVE_COMPARATOR

Elbow Fracture Fixation

Intervention Type PROCEDURE

Interventions

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Elbow Fracture Fixation

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* Incomplete or inaccessable chart data
Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ann & Robert H Lurie Children's Hospital of Chicago

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Santhanam Suresh, MD

Role: PRINCIPAL_INVESTIGATOR

Ann & Robert H Lurie Children's Hospital of Chicago

Locations

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

Chicago, Illinois, United States

Site Status

Countries

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United States

References

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Suresh S, Sarwark JP, Bhalla T, Janicki J. Performing US-guided nerve blocks in the postanesthesia care unit (PACU) for upper extremity fractures: is this feasible in children? Paediatr Anaesth. 2009 Dec;19(12):1238-40. doi: 10.1111/j.1460-9592.2009.03182.x. No abstract available.

Reference Type BACKGROUND
PMID: 20017868 (View on PubMed)

Steinfeldt J, Robison T, Przybylo HJ. Placement of an US-guided supraclavicular block postoperatively in children: can we make this easy? Paediatr Anaesth. 2010 Aug;20(8):780-1. doi: 10.1111/j.1460-9592.2010.03355.x. No abstract available.

Reference Type BACKGROUND
PMID: 20670249 (View on PubMed)

Other Identifiers

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2014-15849

Identifier Type: -

Identifier Source: org_study_id

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