Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
40 participants
INTERVENTIONAL
2015-10-31
2016-01-31
Brief Summary
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One half of the participants will receive an osteopathic manuel treatment in order to stimulate the relevant segments, the other half will receive no treatment.
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Detailed Description
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A follow up blood screening (TSH, fT4) will be done. The results of both groups will be compared.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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OMT-Group
The OMT-group will get an osteopathic treatment once a week for 1 hour for 5 weeks. The blood will be screened again after the treatment.
OMT
Manuel osteopathic treatment of the spine
Controll Group
This group will receive no treatment. A blood screening is made again after 5 weeks.
No interventions assigned to this group
Interventions
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OMT
Manuel osteopathic treatment of the spine
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Increased thyroxin-binding globulin
* Decreased thyroxin-binding globulin
* Binding inhibitors
* Inherited Salicylates
* Pregnancy
* Androgens
* Furosemide
* Neonatal state
* Anabolic steroids
* Free fatty acids
* Estrogens
* Glucocorticoids
* Phenytoin
* Hepatitis
* Severe illness
* Carbamazepine
* Porphyria
* Hepatic failure
* nonsteroidal antiinflammatory drug (variable, transient)
* Heroin
* Nephrosis
* Heparin
* Methadone
* Nicotinic acid
* Mitotane L-Asparaginase
* 5-Fluorouracil
* SERMS (e.g., tamoxifen, raloxifene)
* Perphenazine
* spinal pathologies
18 Years
65 Years
FEMALE
No
Sponsors
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Emanuel Amier Diekmann
INDIV
Responsible Party
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Emanuel Amier Diekmann
DO
Principal Investigators
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Emanuel Diekmann, DO
Role: PRINCIPAL_INVESTIGATOR
Praxis fuer Osteopathy
Central Contacts
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Other Identifiers
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17-5-2015
Identifier Type: -
Identifier Source: org_study_id
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