Assessing Peripheral Nerve Block Scoring Systems for Intra-Operative and Post-Operative Analgesia

NCT ID: NCT02041806

Last Updated: 2014-01-22

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

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-07-31

Study Completion Date

2014-06-30

Brief Summary

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The purpose of this study is to determine if Peripheral Nerve Block scoring systems are effective in predicting the achievement of intra-operative anaesthesia and post-operative analgesia.

Detailed Description

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Upper and lower extremity surgery is particularly suited to regional anaesthesia. Peripheral nerve blocks (PNB) can produce surgical anaesthesia in less than 30 minutes. PNBs have been associated with early outcome improvements when surgery is conducted awake or with light sedation. These benefits include reduced nausea and vomiting, improved patient satisfaction and accelerated recovery room and hospital discharge. PNBs can also provide effective postoperative pain relief.

Currently there is no globally accepted standard by which to assess when surgical anaesthesia has been achieved following administration of PNBs. The decision as to when adequate surgical anaesthesia has been achieved and when surgery can then proceed is usually left to the discretion of the anaesthetist. The anaesthetist can assess nerve blockade though several motor and sensory function tests: cold, heat, touch and pinprick sensitivity. Several scoring systems have been described using these tests to estimate when surgical anaesthesia has been achieved but none have been independently validated outside of the original studies in which they have been described.

Conditions

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Complication of Anesthesia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* American Society of Anesthesiologists Grade I-IV

Exclusion Criteria

* Contraindications to regional anesthesia
* Language barrier
* Existence of neurologic disease affecting the operative site
* Severe psychiatric disease
* Pregnancy
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Adelaide and Meath Hospital

OTHER

Sponsor Role lead

Responsible Party

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Dr Patrick Conroy

Consultant Anaesthesia

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Patrick H Conroy

Role: PRINCIPAL_INVESTIGATOR

The Adelaide and Meath Hospital

Locations

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Tallaght Hospital

Dublin, , Ireland

Site Status RECRUITING

Countries

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Ireland

Central Contacts

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Patrick Conroy, MB

Role: CONTACT

00353852785308

Facility Contacts

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Patrick Conroy

Role: primary

Other Identifiers

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SS/2013/81

Identifier Type: -

Identifier Source: org_study_id

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