Assessment of Spread of Transversus Abdominis Plane Block
This study has been completed.
Sponsor:
Herlev Hospital
Collaborator:
Glostrup University Hospital, Copenhagen
Information provided by:
Herlev Hospital
ClinicalTrials.gov Identifier:
NCT01024868
First received: December 2, 2009
Last updated: May 3, 2010
Last verified: December 2009
| Tracking Information | |||||
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| First Received Date ICMJE | December 2, 2009 | ||||
| Last Updated Date | May 3, 2010 | ||||
| Start Date ICMJE | December 2009 | ||||
| Primary Completion Date | March 2010 (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 NCT01024868 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 | Assessment of Spread of Transversus Abdominis Plane Block | ||||
| Official Title ICMJE | Assessment of Spread of Transversus Abdominis Plane Block After Administration of 20 ml Ropivacaine 0,5% Bilaterally | ||||
| Brief 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. |
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| Detailed Description | Not Provided | ||||
| Study Type ICMJE | Observational | ||||
| Study Design ICMJE | Observational Model: Case-Only Time Perspective: Prospective |
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| Target Follow-Up Duration | Not Provided | ||||
| Biospecimen | Not Provided | ||||
| Sampling Method | Non-Probability Sample | ||||
| Study Population | Patients undergoing abdominal surgery |
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| Condition ICMJE | Transversus Abdominis Plane Block | ||||
| Intervention ICMJE | Drug: Ropivacaine 0,5%
Injection of ropivacaine 0,5% 20 ml bilaterally before surgery |
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| Study Group/Cohort (s) | TAP block
Patients before undergoing laparoscopic or other abdominal surgery
Intervention: Drug: Ropivacaine 0,5% |
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| Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Estimated Enrollment ICMJE | 20 | ||||
| Completion Date | Not Provided | ||||
| Primary Completion Date | March 2010 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | Denmark | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT01024868 | ||||
| Other Study ID Numbers ICMJE | TDTSG-1 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Dr Anja U. Mitchell, Herlev University Hospital, Copenhagen | ||||
| Study Sponsor ICMJE | Herlev Hospital | ||||
| Collaborators ICMJE | Glostrup University Hospital, Copenhagen | ||||
| Investigators ICMJE |
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| Information Provided By | Herlev Hospital | ||||
| Verification Date | December 2009 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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