Description of the Association of Signs and Symptoms Present at Acromegaly Diagnosis (ACRO-POLIS)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT02012127
Recruitment Status : Completed
First Posted : December 16, 2013
Last Update Posted : July 29, 2014
Information provided by (Responsible Party):

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

Condition or disease

Study Type : Observational
Actual Enrollment : 648 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Description of the Associations of Sign-and-symptom at Acromegaly Diagnosis.
Study Start Date : September 2013
Actual Primary Completion Date : June 2014
Actual Study Completion Date : June 2014

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Acromegalic patients

Primary Outcome Measures :
  1. Description of the most characteristic sign-and-symptom associations of acromegaly, collected by a patient questionnaire. [ Time Frame: At the time of patient diagnosis, up to 3 months ]

Secondary Outcome Measures :
  1. Description of demographic and clinical characteristics of patients with acromegaly, collected by a patient questionnaire. [ Time Frame: At the time of patient diagnosis, up to 3 months ]

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Acromegalic patients

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT02012127

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, France
Sponsors and Collaborators
Study Director: Karima Menia, PhD Ipsen

Responsible Party: Ipsen Identifier: NCT02012127     History of Changes
Other Study ID Numbers: 8-54-52030-266
First Posted: December 16, 2013    Key Record Dates
Last Update Posted: July 29, 2014
Last Verified: July 2014

Additional relevant MeSH terms:
Signs and Symptoms
Bone Diseases, Endocrine
Bone Diseases
Musculoskeletal Diseases
Pituitary Diseases
Hypothalamic Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Endocrine System Diseases