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Study of Metabolic Effects of Pregnancy in Women With Cystic Fibrosis

NCT00014768 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 36

Last updated 2005-06-24

No results posted yet for this study

Summary

OBJECTIVES: I. Compare the clinical status of pregnant vs non-pregnant women with cystic fibrosis.

II. Determine glucose tolerance during each trimester of pregnancy in these women.

III. Evaluate peripheral insulin sensitivity in these women. IV. Evaluate whole body protein turnover and hepatic glucose production in these women.

V. Determine resting energy expenditure in these women.

Conditions

Interventions

DRUG

glucose

DRUG

insulin

DRUG

leucine

Sponsors & Collaborators

  • University of Utah

    collaborator OTHER

  • National Center for Research Resources (NCRR)

    lead NIH

Principal Investigators

  • Dana S. Hardin · University of Utah

Eligibility

Min Age
0 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2001-02-28

Countries

  • United States

Study Locations

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Entities

Drugs
Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00014768 on ClinicalTrials.gov