Medical Review: Hand Surgery After Local Block Versus Non-block

NCT ID: NCT01110759

Last Updated: 2013-11-01

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

COMPLETED

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-08-31

Study Completion Date

2011-07-31

Brief Summary

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In this study, the effects of local block vs non block will be assessed with respect to postoperative outcomes (such as pain score, and recovery profiles) in outpatients after hand surgery.

Detailed Description

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Analyzing medical records and through a telephone questionnaire, in a retrospective and prospective review respectively.

Conditions

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Carpal Tunnel Syndrome

Keywords

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pain management ambulatory surgery opioid local anesthesia hand surgery postoperative pain

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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Under Local Infiltration

No interventions assigned to this group

Under Peripheral Nerve Block

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* 18-80 years old
* Outpatients who underwent hand surgery under peripheral nerve block or local infiltration alone
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cedars-Sinai Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Ronald Wender

Chairman, Department of Anesthesiology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ronald H Wender, MD

Role: PRINCIPAL_INVESTIGATOR

Cedars-Sinai Medical Center

Locations

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Cedars Sinai Medical Center

Los Angeles, California, United States

Site Status

Countries

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United States

Other Identifiers

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Pro00019315

Identifier Type: -

Identifier Source: org_study_id