NCT02893436

Brief Summary

The purpose is to calculate the time for an optimal recovery (T4/T1 \> 0.9) from the moment when 2 responses to double burst stimulation are visually identical and this for 95% of patients.

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
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Apr 2014

Typical duration 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

April 1, 2014

Completed
2.4 years until next milestone

First Submitted

Initial submission to the registry

August 31, 2016

Completed
1 day until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2016

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 8, 2016

Completed
Last Updated

September 8, 2016

Status Verified

August 1, 2016

Enrollment Period

2.4 years

First QC Date

August 31, 2016

Last Update Submit

September 2, 2016

Conditions

AnesthesiaSurgery

Outcome Measures

Primary Outcomes (1)

  • Time interval between the moment when DBSs are visually identical and the T4/T1 ratio is > 0.9

    measured with TOF-Watch Sx

    day 0

Study Arms (1)

Curarized patients

Procedure: Surgery with tracheal intubation curarisation

Interventions

Surgery with tracheal intubation curarisationPROCEDURE
Curarized patients

Eligibility Criteria

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

Patient curarised at Nancy Hospital

You may qualify if:

  • ASA score 1-3
  • Needing a surgery with tracheal intubation curarisation

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHRU Nancy

Vandœuvre-lès-Nancy, France

RECRUITING

MeSH Terms

Interventions

Surgical Procedures, Operative

Study Officials

  • Denis Schmartz

    CHRU Nancy, France

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Denis Schmartz

CONTACT

d.schmartz@chru-nancu.fr

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 31, 2016

First Posted

September 8, 2016

Study Start

April 1, 2014

Primary Completion

September 1, 2016

Study Completion

September 1, 2016

Last Updated

September 8, 2016

Record last verified: 2016-08

Locations

FR(1)