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

The Effectiveness of Peripheral Nerve Block Scoring Systems in Predicting the Success of a Block for Intra-Operative and Post-Operative Analgesia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02041806
Enrollment
40
Registered
2014-01-22
Start date
2013-07-31
Completion date
2014-06-30
Last updated
2014-01-22

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

Conditions

Complication of Anesthesia

Brief summary

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

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.

Interventions

None listed

Sponsors

The Adelaide and Meath Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frame
Predictive value of block assessment score30 mins post block completion

Countries

Ireland

Contacts

Primary ContactPatrick Conroy, MB
P_W_C@hotmail.com00353852785308

Outcome results

None listed

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