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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02827058
Other study ID # 2016/140
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date March 2016
Est. completion date May 1, 2018

Study information

Verified date April 2020
Source Central Norway Regional Health Authority
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether injection needle pen point type 'PP Gauge 25' should be recommended as a primary choice of needle (in stead of 'PP Gauge 27') for healthy pregnant women who at delivery (vaginal or cesarean section) get spinal anesthesia.


Recruitment information / eligibility

Status Terminated
Enrollment 65
Est. completion date May 1, 2018
Est. primary completion date May 1, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- healthy

- pregnant

- spinal anesthesia at delivery (vaginal delivery or cesarean section emergency grade 2-4)

- informed consent

Exclusion Criteria:

- chronic headache

- (attempt to) epidural anesthesia

Study Design


Related Conditions & MeSH terms


Intervention

Device:
G25 pencil point needle

G27 pencil point needle


Locations

Country Name City State
Norway Østfold Hospital Fredrikstad
Norway Levanger Hospital Levanger

Sponsors (2)

Lead Sponsor Collaborator
Central Norway Regional Health Authority Sykehuset Ostfold

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of attempts until successful injection 0 (injection time before delivery)
Secondary incidence of post dural puncture headache 48 hrs
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