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Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2013-000950-23-FR
Enrollment
240
Registered
2013-07-24
Start date
2013-05-14
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

MedDRA version: 14.1 Level: LLT Classification code 10043777 Term: Thyroidectomy total System Organ Class: 100000004865

Interventions

Trade Name: PULMICORT Product Name: Budésonide Pharmaceutical Form: Nebuliser suspension

Sponsors

CHU Dijon
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 240 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 240

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Main Objective: ;Secondary Objective: ;Primary end point(s): ;Timepoint(s) of evaluation of this end point: Before and after surgery then every day until its exit

Secondary

MeasureTime frame
Timepoint(s) of evaluation of this end point: Before and after surgery then every day until its exit

Countries

France

Contacts

Public ContactChef de projets recherche

CHU Dijon

maud.carpentier@chu-dijon.fr038029561833

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026