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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02012127
Other study ID # A-54-52030-266
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2013
Est. completion date June 2014

Study information

Verified date August 2019
Source Ipsen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to describe most characteristic association of signs and symptoms present at the time of acromegaly diagnosis.


Recruitment information / eligibility

Status Completed
Enrollment 648
Est. completion date June 2014
Est. primary completion date June 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patient (greater than or equal to 18 years old)

- Patient with acromegaly, diagnosed for less than 5 years

Exclusion Criteria:

- Patient who have objected to the collection of his/her data

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Hôpital Sud Amiens
France CHU Besançon Hôpital Jean Minjoz Besançon
France Hôpital la Cavale Blanche Brest
France Chu Cote de Nacre Caen
France Hôpital Henri Mondor Creteil
France Chu de Grenoble Hôpital Albert Michallon Grenoble
France Hôpital Claude Huriez Lille
France Hôpital le Cluzeau Limoges
France Hôpital Neuro-cardiologique Lyon
France Hôpital de la Timone Marseille
France Hôpital Lepeyronie Montpellier
France Hôpitaux de Brabois Nancy
France CHR Orléans - Hôpital la Source Orléans
France CH de Bicetre Paris
France CH Pitie Salpetreire Paris
France Hôpital Lariboisiere Paris
France Hôpital Haut Leveque Pessac
France CHU Reims - Hôpital Robert Debre Reims
France Hôpital Sud Anne de Bretagne Rennes
France CHU Rouen - Hôpital de Bois Guillaume Rouen
France Hôptital Nord Saint Etienne
France Hôpital Civil Strasbourg
France Hôpital de Hautepierre Strasbourg
France Hôpital Larrey Toulouse
France CHU Bretonneau Tours

Sponsors (1)

Lead Sponsor Collaborator
Ipsen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Description of the most characteristic sign-and-symptom associations of acromegaly, collected by a patient questionnaire. At the time of patient diagnosis, up to 3 months
Secondary Description of demographic and clinical characteristics of patients with acromegaly, collected by a patient questionnaire. At the time of patient diagnosis, up to 3 months
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