Evaluation of the Physicians and Patients Experience of Fetal Scalp Sampling

This study has been completed.

Sponsor:

Information provided by (Responsible Party):

Maria Jonsson, Uppsala University Hospital

ClinicalTrials.gov Identifier:

NCT01277588

First received: January 14, 2011

Last updated: January 16, 2012

Last verified: January 2012

History of Changes

Tracking Information
First Received Date ^ICMJE	January 14, 2011
Last Updated Date	January 16, 2012
Start Date ^ICMJE	August 2010
Primary Completion Date	August 2011 (final data collection date for primary outcome measure)
Current Primary Outcome Measures ^ICMJE	Not Provided
Original Primary Outcome Measures ^ICMJE	Not Provided
Change History	Complete list of historical versions of study NCT01277588 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE	Not Provided
Original Secondary Outcome Measures ^ICMJE	Not Provided
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Evaluation of the Physicians and Patients Experience of Fetal Scalp Sampling
Official Title ^ICMJE	Not Provided
Brief Summary	During labor, fetal scalp sampling is performed if the CTG registration is abnormal. The test is performed with the woman in the supine position and is generally described as a difficult and cumbersome procedure.
Detailed Description	Women who were subjected to fetal scalp sampling are asked to fill in a questionnaire within 24 hours after delivery. The questionnaire deals with how the woman experienced the testing procedure. Physicans who performed the test are asked to fill in a questionnaire within 24 hours after delivery. The questionnaire deals with how the physician experienced the testing procedure.
Study Type ^ICMJE	Observational
Study Design ^ICMJE	Observational Model: Case-Only Time Perspective: Prospective
Target Follow-Up Duration	Not Provided
Biospecimen	Not Provided
Sampling Method	Non-Probability Sample
Study Population	Women who are subjected to fetal scalp sampling during labor Physicians performning fetal scalp sampling
Condition ^ICMJE	Questionnaire Fetal Scalp Sampling
Intervention ^ICMJE	Not Provided
Study Group/Cohort (s)	Patient Physcician
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Completed
Enrollment ^ICMJE	51
Completion Date	August 2011
Primary Completion Date	August 2011 (final data collection date for primary outcome measure)
Eligibility Criteria ^ICMJE	Inclusion Criteria: fetal scalp sampling during labor Exclusion Criteria: non-proficiency in the Swedish language
Gender	Female
Ages	18 Years and older
Accepts Healthy Volunteers	No
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	Sweden

Administrative Information
NCT Number ^ICMJE	NCT01277588
Other Study ID Numbers ^ICMJE	UAS2010/003
Has Data Monitoring Committee	No
Responsible Party	Maria Jonsson, Uppsala University Hospital
Study Sponsor ^ICMJE	Uppsala University Hospital
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	Uppsala University Hospital
Verification Date	January 2012
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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