Evaluation of the Physicians and Patients Experience of Fetal Scalp Sampling

Questionnaire Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01277588
• Other study ID #: UAS2010/003
• Status: Completed
• Phase: N/A
• First received: January 14, 2011
• Last updated: January 16, 2012
• Start date: August 2010
• Est. completion date: August 2011

Study information

• Verified date: January 2012
• Source: Uppsala University Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Sweden: Ethics commitee
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 51
• Est. completion date: August 2011
• Est. primary completion date: August 2011
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• fetal scalp sampling during labor

Exclusion Criteria:

• non-proficiency in the Swedish language

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

• Fetal Scalp Sampling
• Questionnaire

Locations

Country	Name	City	State
Sweden	Department of obstetrics and gynecology	Uppsala

Sponsors (1)

Lead Sponsor	Collaborator
Uppsala University Hospital

Country where clinical trial is conducted

Sweden,