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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00151099
Other study ID # 03-Anast-05
Secondary ID
Status Withdrawn
Phase Phase 4
First received September 7, 2005
Last updated December 17, 2015
Start date September 2005
Est. completion date December 2007

Study information

Verified date August 2007
Source University Hospital Muenster
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

The purpose of the study is to determine whether the oral administration of a high caloric drink with protein decreases the postoperative nausea and vomiting in patients with dysgnathia.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Patients with surgery for dysgnathia

Exclusion Criteria:

- Diabetes mellitus

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms

  • Postoperative Nausea and Vomiting

Intervention

Drug:
high caloric drink with protein


Locations

Country Name City State
Germany Department of Anesthesiology and Intensive Care, University Hospital Münster Münster

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Muenster

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary gastric residual at induction of anesthesia
Secondary postoperative wellness
Secondary thermoregulation
See also
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