- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00674726
Study on the Difference of Axilo-rectal Temperature in Appendicitis
October 29, 2012 updated by: MARCELO A. BELTRAN, M.D., Cirujanos la Serena
Prospective Study on the Difference of Axilar-rectal Temperature in Acute Appendicitis
The investigators are studying prospectively the difference in axilo-rectal temperature in patients with acute appendicitis and using as a control group patients consulting with acute gastroenteritis at our emergency unit.
Study Overview
Status
Withdrawn
Conditions
Intervention / Treatment
Study Type
Observational
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
IV Region
-
La Serena, IV Region, Chile
- Hospital De La Serena - Emergency Unit
-
La Serena, IV Region, Chile
- Hospital de La Serena
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
15 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients consulting in the emergency unit with acute appendicitis or acute gastroenteritis
Description
Inclusion Criteria:
- Patients with acute appendicitis
- Patients with acute gastroenteritis
- Patients older than 15 years of age
Exclusion Criteria:
- Other acute abdominal diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Group I
Patients with acute appendicitis
|
Measurement of axilo-rectal temperature
|
Group II
Patients with acute gastroenteritis
|
Measurement of axilo-rectal temperature
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
The real difference in axilo-rectal temperature in patients with acute appendicitis
Time Frame: 6 hours
|
6 hours
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
The differences in axilo-rectal temperature between patients with acute appendicitis and acute gastroenteritis
Time Frame: 6 hours
|
6 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: MARCELO A BELTRAN, M.D., Hospital de La Serena
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2008
Primary Completion (Actual)
May 1, 2008
Study Completion (Actual)
July 1, 2008
Study Registration Dates
First Submitted
May 6, 2008
First Submitted That Met QC Criteria
May 7, 2008
First Posted (Estimate)
May 8, 2008
Study Record Updates
Last Update Posted (Estimate)
October 31, 2012
Last Update Submitted That Met QC Criteria
October 29, 2012
Last Verified
October 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HLS-002-05-08
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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