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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01024868
Other study ID # TDTSG-1
Secondary ID
Status Completed
Phase N/A
First received December 2, 2009
Last updated May 3, 2010
Start date December 2009

Study information

Verified date December 2009
Source Herlev Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Observational

Clinical Trial Summary

For the purpose of assessing the spread of the local anaesthetic after injecting it between abdominal muscles on both sides, the investigators will test if the patient can feel a change in the perception of cold and warm, as well as being pricked with a blunt needle. The investigators will also take several blood samples, together with routine samples, to measure the concentration of the local anesthetic in the blood.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date
Est. primary completion date March 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- undergo abdominal surgery, eligible for TAP block, over 18, BMI 20-40

Exclusion Criteria:

- does not speak danish, does not consent, does not fulfill inclusion criteria

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Transversus Abdominis Plane Block

Intervention

Drug:
Ropivacaine 0,5%
Injection of ropivacaine 0,5% 20 ml bilaterally before surgery

Locations

Country Name City State
Denmark Herlev University Hospital Herlev

Sponsors (2)

Lead Sponsor Collaborator
Herlev Hospital Glostrup University Hospital, Copenhagen

Country where clinical trial is conducted

Denmark, 

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