ID

23708

Description

Responsible Party: Johannes W. Dietrich, MD, Senior consultant endocrinologist, Ruhr University of Bochum ClinicalTrials.gov Identifier: NCT01145040 History of Changes Other Study ID Numbers: TFC-UK10 3718-10 ( Other Identifier: Ethics commission of the Ruhr University of Bochum ) U1111-1122-3273 ( Registry Identifier: WHO ICTRP Universal Trial Number (UTN) ) DRKS00003153 ( Registry Identifier: DRKS (German Clinical Trials Register) ) Study First Received: June 14, 2010 Last Updated: April 24, 2017 NOMOTHETICOS: Nonlinear Modelling of Thyroid Hormones' Effect on Thyrotropin Incretion in Confirmed Open-loop Situation (NOMOTHETICOS) ODM derived from: https://clinicaltrials.gov/ct2/show/NCT01145040

Lien

https://clinicaltrials.gov/ct2/show/NCT01145040

Mots-clés

Versions (1)
  1. 11/07/17 11/07/17 -
Téléchargé le

11 luglio 2017

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Thyroid Disease NCT01145040 DRKS00003153

Anglais

Eligibility Thyroid Disease NCT01145040 DRKS00003153

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Ages Eligible for Study: 14 Years and older (Child, Adult, Senior)
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
Outpatients with disconnected feedback control due to the following conditions: - Overt primary hypothyroidism with TSH level over 10 mU/l and FT4 level below 0.5 ng/l (Partition 1)
Description

Hypothyroidism

Type de données

boolean

Alias
UMLS CUI [1]
C0020676
Outpatients with disconnected feedback control due to the following conditions: - Overt primary hyperthyroidism with TSH level below 0.1 mU/l and FT4 level over 25 ng/l (Partition 3)
Description

Hyperthyroidism

Type de données

boolean

Alias
UMLS CUI [1]
C0020550
Outpatients with disconnected feedback control due to the following conditions: - All other constellations, if the patient receives substitution therapy with more 1.75 µg Levothyroxin per kg of body mass (Partition 2).
Description

Levothyroxine substitution

Type de données

boolean

Alias
UMLS CUI [1]
C0040165
System in equilibrium (e.g. unchanged substitution dose over the past six weeks)
Description

Equilibrium

Type de données

boolean

Alias
UMLS CUI [1]
C0014653
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Healthy Volunteers
Description

Control Group

Type de données

boolean

Alias
UMLS CUI [1]
C0009932
Pituitary or hypothalamic dysfunction
Description

Pituitary or hypothalamic dysfunction

Type de données

boolean

Alias
UMLS CUI [1]
C0281947
UMLS CUI [2]
C0751230
Severe illness that may be associated with euthyroid sick syndrome (non-thyroidal illness syndrome)
Description

Comorbidity

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
Medication influencing pituitary function
Description

Drug Interactions

Type de données

boolean

Alias
UMLS CUI [1]
C0687133
Pregnancy
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
Missing consent for participation in the study
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
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Similar models

Eligibility Thyroid Disease NCT01145040 DRKS00003153

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Age
Item
Ages Eligible for Study: 14 Years and older (Child, Adult, Senior)
boolean
C0001779 (UMLS CUI [1])
Hypothyroidism
Item
Outpatients with disconnected feedback control due to the following conditions: - Overt primary hypothyroidism with TSH level over 10 mU/l and FT4 level below 0.5 ng/l (Partition 1)
boolean
C0020676 (UMLS CUI [1])
Hyperthyroidism
Item
Outpatients with disconnected feedback control due to the following conditions: - Overt primary hyperthyroidism with TSH level below 0.1 mU/l and FT4 level over 25 ng/l (Partition 3)
boolean
C0020550 (UMLS CUI [1])
Levothyroxine substitution
Item
Outpatients with disconnected feedback control due to the following conditions: - All other constellations, if the patient receives substitution therapy with more 1.75 µg Levothyroxin per kg of body mass (Partition 2).
boolean
C0040165 (UMLS CUI [1])
Equilibrium
Item
System in equilibrium (e.g. unchanged substitution dose over the past six weeks)
boolean
C0014653 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])
Pituitary or hypothalamic dysfunction
Item
Pituitary or hypothalamic dysfunction
boolean
C0281947 (UMLS CUI [1])
C0751230 (UMLS CUI [2])
Comorbidity
Item
Severe illness that may be associated with euthyroid sick syndrome (non-thyroidal illness syndrome)
boolean
C0009488 (UMLS CUI [1])
Drug Interactions
Item
Medication influencing pituitary function
boolean
C0687133 (UMLS CUI [1])
Pregnancy
Item
Pregnancy
boolean
C0032961 (UMLS CUI [1])
Informed Consent
Item
Missing consent for participation in the study
boolean
C0021430 (UMLS CUI [1])
Retour au début de la page 

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