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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01787266
Other study ID # PGQ2013
Secondary ID 129/12-303.0
Status Completed
Phase
First received January 31, 2013
Last updated April 5, 2018
Start date January 2013
Est. completion date December 2014

Study information

Verified date April 2018
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to:

1. describe degree of symptoms and disability during and after pregnancy

2. to examine if women with pelvic girdle pain are able to correctly mark their pain location on a pain drawing

3. to examine the responsiveness of The Pelvic Girdle Questionnaire


Recruitment information / eligibility

Status Completed
Enrollment 800
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Pregnancy week 32-36

- Understand and read/write a questionnaire in Norwegian or English

Exclusion Criteria:

- Not able to understand and fill in a questionnaire

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Norway Oslo University Hospital Oslo

Sponsors (1)

Lead Sponsor Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Other Short Form -8 (SF-8) 10 weeks postpartum
Primary the pelvic girdle questionnaire 10 weeks postpartum
Secondary Pain intensity, Numeric rating scale 10 weeks postpartum
See also
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