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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01105143
Other study ID # EA 20100415
Secondary ID
Status Completed
Phase N/A
First received April 14, 2010
Last updated December 18, 2017
Start date March 2012
Est. completion date May 2017

Study information

Verified date December 2017
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators here propose to perform a prospective randomized intervention trial in post-menopausal women to investigate the endocrine network, which contributes to the changes in skeletal muscle mass during weight loss.


Recruitment information / eligibility

Status Completed
Enrollment 81
Est. completion date May 2017
Est. primary completion date May 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

- BMI > 27 kg/m2 (adults)

- postmenopausal state

Exclusion criteria:

- weight loss of more than 5kg in the last 2 months x

- unhealthy patients with: severe chronic diseases including cancer within the last 5 years, severe heart disease, severe impairment of hepatic or renal function, severe anaemia or disturbed coagulation

- eating disorders or any other psychiatric condition that would interact with the trial intervention

- malabsorption

- acute or chronic infections

- severe hypertension

- myopathy

- food allergies

- any other uncontrolled endocrine disorder

- changes of smoking habits, diets or medication that strongly affects energy homeostasis within the last 3 months prior to study inclusion

Study Design


Intervention

Behavioral:
multimodal lifestyle intervention
multimodal lifestyle intervention will be performed to reduce body weight
placebo
no intervention, only follow up

Locations

Country Name City State
Germany Charite Berlin

Sponsors (2)

Lead Sponsor Collaborator
Charite University, Berlin, Germany German Research Foundation

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Other FFA during negative energy balance and during stabilized modification of body composition after weight loss. Measurement of fatty acids at baseline, during negative energy balance, during stabilized modification of body composition after weight loss and during follow up. 12 months
Other Metanephrines during negative energy balance and during stabilized modification of body composition after weight loss. Measurement of metanephrines at baseline, during negative energy balance, during stabilized modification of body composition after weight loss and during follow up. 12 months
Other Leptin during negative energy balance and during stabilized modification of body composition after weight loss. Measurement of leptin at baseline, during negative energy balance, during stabilized modification of body composition after weight loss and during follow up. 12 months
Other Cortisol during negative energy balance and during stabilized modification of body composition after weight loss. Measurement of cortisol at baseline, during negative energy balance, during stabilized modification of body composition after weight loss and during follow up. 12 months
Other Follistatin during negative energy balance and during stabilized modification of body composition after weight loss. Measurement of follistatin at baseline, during negative energy balance, during stabilized modification of body composition after weight loss and during follow up. 12 months
Other Adiponectin during negative energy balance and during stabilized modification of body composition after weight loss. Measurement adiponectin at baseline, during negative energy balance, during stabilized modification of body composition after weight loss and during follow up. 12 months
Other Natriuretic peptide during negative energy balance and during stabilized modification of body composition after weight loss. Measurement of natriuretic peptide at baseline, during negative energy balance, during stabilized modification of body composition after weight loss and during follow up. 12 months
Other IGF-1 during negative energy balance and during stabilized modification of body composition after weight loss. Measurement of IGF-1 at baseline, during negative energy balance, during stabilized modification of body composition after weight loss and during follow up. 12 months
Other Analysis of predictive impact of several hormonal and metabolic parameters on body weight regain, course of insulin sensitivity and metabolism The effect of measured parameters (see other endpoints) on long-term course of BMI, muscle mass, insulin sensitivity and energy expenditure will be analyzed using mathematical models 24 months
Primary Changes of myocellular insulin sensitivity (hyperinsulinemic clamp) during negative energy balance and during stabilized modification of body composition after weight loss. Analysis of myocellular insulin sensitivity by hyperinsulinemic clamp in mg•kg-1•min-1/(mU•L-1) 4 months
Primary Changes of skeletal muscle mass (air displacement plethysmography) during negative energy balance and during stabilized modification of body composition after weight loss. Analysis of muscle mass (in % of body weight) 4 months
Secondary Effects on energy expenditure Measurement of energy expenditure (kcal/d), postprandial thermogenesis (%) and respiratory coefficient 4 months
Secondary Effects on myocellular and adipose tissue metabolism and substrate utilization Measurement of myocellular and adipose metabolism using microdialysis (glycerol (µmol/l), lactate (mmol/l), pyruvate (µmol/l), glucose (mmol/l)) during oral glucose load (180 minutes) 4 months
Secondary Effects on myocellular and adipose tissue mRNA expression Analysis of myocellular and adipose mRNA expression (RNA sequencing) in counts 4 months
Secondary Weight regain Analysis of body weight regain (BMI; kg/m2) during follow up 24 months
Secondary Fat mass Analysis of body fat (kg and %) 24 months
Secondary Measurement of human gut microbiome at baseline, during weight loos, after weight loss (negative energy balance) and during stabilized modification of body composition 4 weeks after weight loss 16S rRNA sequencing and/or shotgun metagenomic pyrosequencing of the gut microbiota for assessment of microbiota composition and gene abundances. 4 months
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