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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02409017
Other study ID # 690224-2
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date April 2015
Est. completion date July 2016

Study information

Verified date September 2019
Source WellSpan Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess which of two commonly utilized insulin drip protocols has better outcomes when used during the labor process.


Recruitment information / eligibility

Status Terminated
Enrollment 20
Est. completion date July 2016
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- a. Pregnant patients with either pre-existing diabetes or gestational diabetes type A2 who require insulin for euglycemia during labor and delivery

Exclusion Criteria:

- a. Those patients who decline participation

- b. Patients less than age 18 at the time of enrollment will be excluded to protect this vulnerable patient population c. Those patients who cannot be consented d. Patients scheduled for cesarean delivery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Insulin drip


Locations

Country Name City State
United States WellSpan York Hospital York Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
WellSpan Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mean maternal glucose Labor
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