- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03721250
Comparison of Thoracic Epidural Analgesia and Intercostal Blockade in Patients Undergoing Thoracotomy
February 27, 2020 updated by: CIGDEM YILDIRIM GUCLU, Ankara University
Postoperative pain is an important issue after thoracotomy operations.
Thoracic epidural analgesia is most popular analgesic method, but sometimes it is not sufficient for pain.
This study is designed to compare intercostal block with thoracic epidural analgesia in patients undergoing thoracotomy
Study Overview
Study Type
Observational
Enrollment (Actual)
50
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
-
-
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Ankara, Turkey, 06550
- Ankara University
-
-
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
16 years to 63 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patients undergoing thoracotomy
Description
Inclusion Criteria:
lung cancer
Exclusion Criteria:
patient refusal bleeding diathesisi emergency cases
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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: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
thoracic epidural
patients receiving thoracic epidural
|
thoracic epidural analgesia
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
verbal analog score
Time Frame: postoperative 24 hour
|
postoperative 24 hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
December 14, 2018
Primary Completion (Actual)
March 4, 2019
Study Completion (Actual)
April 22, 2019
Study Registration Dates
First Submitted
October 23, 2018
First Submitted That Met QC Criteria
October 24, 2018
First Posted (Actual)
October 26, 2018
Study Record Updates
Last Update Posted (Actual)
February 28, 2020
Last Update Submitted That Met QC Criteria
February 27, 2020
Last Verified
February 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Ank230918
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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