NCT02041806

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jul 2013

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2013

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

January 16, 2014

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 22, 2014

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2014

Completed
Last Updated

January 22, 2014

Status Verified

January 1, 2014

Enrollment Period

11 months

First QC Date

January 16, 2014

Last Update Submit

January 18, 2014

Conditions

Complication of Anesthesia

Outcome Measures

Primary Outcomes (1)

  • Predictive value of block assessment score

    30 mins post block completion

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients undergoing orthopaedic or vascular surgery who would receive a peripheral nerve block as part of their care.

You may qualify if:

  • American Society of Anesthesiologists Grade I-IV

You may not qualify if:

  • Contraindications to regional anesthesia
  • Language barrier
  • Existence of neurologic disease affecting the operative site
  • Severe psychiatric disease
  • Pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tallaght Hospital

Dublin, Ireland

RECRUITING

Study Officials

  • Patrick H Conroy

    The Adelaide and Meath Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Patrick Conroy, MB

CONTACT

00353852785308P_W_C@hotmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Consultant Anaesthesia

Study Record Dates

First Submitted

January 16, 2014

First Posted

January 22, 2014

Study Start

July 1, 2013

Primary Completion

June 1, 2014

Study Completion

June 1, 2014

Last Updated

January 22, 2014

Record last verified: 2014-01

Locations

IE(1)