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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00867022
Other study ID # GESTSYMPIS
Secondary ID
Status Completed
Phase N/A
First received March 20, 2009
Last updated March 20, 2009
Start date August 2004
Est. completion date March 2009

Study information

Verified date March 2009
Source Helsinki University
Contact n/a
Is FDA regulated No
Health authority Finland: Ethics Committee
Study type Observational

Clinical Trial Summary

Through complex hormonal pathways, insulin resistance can lead to the activation of the sympathetic nervous system, and vice versa. Schobel et al. showed that in PE patients, mus-cle sympathetic nerve activity (MSNA) is increased compared with normotensive pregnant and non-pregnant women. Studies assessing heart-rate variability and plasma noradrenalin concentrations also suggest increased sympathetic activity in PE. It has been hypothesized that sympathetic over-activity is a precursor of PE, normally compensated for by vasodilating mechanisms, but resulting in PE when the mechanisms fail. In addition to sympathetic activity, various markers of inflamma-tion are also associated with reduced insulin sensitivity, suggesting that chronic sub-clinical inflamma-tion could be part of the insulin resistance syndrome. The role of sympathetic over-activity and inflammatory markers in gestational diabetes has not been investigated


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date March 2009
Est. primary completion date November 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Clinical diagnosis of gestational diabetes (OGTT) with or without BP > 140/90.

- Pregnant control with normal OGTT-

Exclusion Criteria:

- Smoking

- Uncontrolled hypertension

- Diabetes

- Medication affecting sympathetic activity

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Finland Department of Obstet and Gyn, Helsinki University Hospital Helsinki Uusimaa

Sponsors (1)

Lead Sponsor Collaborator
Helsinki University

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Serum Noradrenalin level No
Secondary Heart rate variability: LF, VLF, HF No
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