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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02282280
Other study ID # SET-STUDY
Secondary ID
Status Completed
Phase N/A
First received October 31, 2014
Last updated December 29, 2015
Start date October 2014
Est. completion date December 2015

Study information

Verified date December 2015
Source Astes
Contact n/a
Is FDA regulated No
Health authority Belgium: The Federal Public Service (FPS) Health, Food Chain Safety and Environment
Study type Observational

Clinical Trial Summary

Observation of the effects of an administration of prilocaine chlorhydrate hyperbare in rachianesthesia among a general surgical population.


Recruitment information / eligibility

Status Completed
Enrollment 380
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 500 consecutive patients with a spinal anesthesia

Exclusion Criteria:

- Patient's refusal

- Age < 18 years

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Drug:
Prilocaine Chlorhydrate
Use of prilocaine in spinal anesthesia

Locations

Country Name City State
Belgium Clinique Saint-Luc Bouge Namur

Sponsors (1)

Lead Sponsor Collaborator
Astes

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of action Baseline No
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