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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01105442
Other study ID # METC2010-18
Secondary ID
Status Completed
Phase N/A
First received April 15, 2010
Last updated July 20, 2011
Start date April 2010
Est. completion date July 2010

Study information

Verified date March 2010
Source Martini Hospital Groningen
Contact n/a
Is FDA regulated No
Health authority The Netherlands: Institutional review board martini hospital groningen
Study type Observational

Clinical Trial Summary

The standard treatment for post operative pain is now bupivacaine + sufentanil. The use of this combination during fast-track colonic surgery leads frequently to post-operative nausea and vomiting and limited mobilisation possibilities. Therefore the department anaesthesiology wants to evaluate the use of a different local anaesthetic: levobupivacaine combined with morphine on demand. The expectation is that the use of levobupivacaine leads to less side effects.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date July 2010
Est. primary completion date June 2010
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who undergo fast-track colonic surgery and with post operative epidural pain treatment

Exclusion Criteria:

- Patients who are admitted to an other ward

- Patients with a spinal catheter

Study Design

Observational Model: Cohort


Locations

Country Name City State
Netherlands Martini Hospital ward 4b Groningen

Sponsors (1)

Lead Sponsor Collaborator
Martini Hospital Groningen

Country where clinical trial is conducted

Netherlands, 

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