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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02979652
Other study ID # 00010254-2016 -016
Secondary ID
Status Recruiting
Phase N/A
First received November 24, 2016
Last updated November 30, 2016
Start date April 2016
Est. completion date January 2018

Study information

Verified date November 2016
Source Hospital Nord
Contact Marc Leone, M.D
Email mleone@ap-hm.fr
Is FDA regulated No
Health authority France: The Commission nationale de l’informatique et des libertés
Study type Observational [Patient Registry]

Clinical Trial Summary

This study is done to estimate prevalence of the main detectable lung and cardiovascular complications by an ultrasound realized in room of post-interventional supervision at the patients whose duration of general anesthesia is superior at one hour after a surgery to risk


Recruitment information / eligibility

Status Recruiting
Enrollment 325
Est. completion date January 2018
Est. primary completion date November 2017
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Physical status score > 1

- Anesthesia of duration > 1 hour

- Visceral, orthopaedic, vascular, thoracic surgery, neurosurgery

Exclusion Criteria:

- Technical incapacity of accessibility to the ultrasound window

- Cardiac or pulmonary transplant

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Departement anesthesie reanimation hopital nord Marseille

Sponsors (1)

Lead Sponsor Collaborator
Hospital Nord

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary cardiac and pulmonary functions cardiac and pulmonary functions will be evaluated by cardiac and pulmonary ultrasound exams for all patient whom have a more than 1 hour surgical intervention 1 hour No
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