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NCT00014768 · ClinicalTrials.gov registry record
Study of Metabolic Effects of Pregnancy in Women With Cystic Fibrosis
A clinical trial, sponsored by National Center for Research Resources (NCRR).
- Terminated
- Registry status
- 36
- Enrollment target
NCT00014768 is a clinical trial that was terminated before completion, run by National Center for Research Resources (NCRR). The registered enrollment target is 36 participants.
The verdict
NCT00014768 was terminated before completion, sponsored by National Center for Research Resources (NCRR).
- TERMINATED
- Registry status
- 36 participants
- Enrollment target
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.
Interventions
- DRUG insulin
- DRUG leucine
- DRUG glucose
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2001-02 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00014768
The ClinicalTrials.gov registry entry for NCT00014768 describes a study currently listed as terminated, categorized as an unspecified phase. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Center for Research Resources (NCRR), which has 94 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which insulin is the first listed.
NCT00014768 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00014768 about?
NCT00014768 is a clinical study titled "Study of Metabolic Effects of Pregnancy in Women With Cystic Fibrosis". 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 gl...
What is the current status of trial NCT00014768?
This trial is currently terminated. The enrollment target is 36 participants. The study started on 2001-02.
What interventions are being tested in trial NCT00014768?
The interventions under investigation include: insulin (DRUG), leucine (DRUG), glucose (DRUG).
Who is sponsoring clinical trial NCT00014768?
This trial is sponsored by National Center for Research Resources (NCRR), which has 94 total clinical trials registered on ClinicalTrials.gov.
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