- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03437096
Postoperative Pain and Venipuncture Pain (venipuncture)
April 3, 2018 updated by: fatih altıparmak, Tokat Gaziosmanpasa University
Association Between Postoperative Pain and Venipuncture Pain in Sleeve Gastrectomy Patients
Association between venipuncture pain and postoperative pain
Study Overview
Detailed Description
Association will be find between venipuncture pain and postoperative pain in sleeve gastrectomy patients.
Also we can study with pain catastrophising scale.
Study Type
Interventional
Enrollment (Anticipated)
1
Phase
- Not Applicable
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
-
-
-
Tokat, Turkey
- Recruiting
- Gaziosmanpasa University
-
Contact:
- Mustafa Süren, MD
-
-
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
18 years to 80 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- sleeve gastrectomy
Exclusion Criteria:
- psychotic illness
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
- Primary Purpose: DIAGNOSTIC
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
OTHER: venipuncture pain
pain during venipuncture
|
postoperative sleeve gastrectomy patients pain
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
numeric rating scale
Time Frame: 3 months
|
pain intensity 0 to 10 during venipuncture
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mustafa Süren, Gaziosmanpasa University
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)
January 15, 2018
Primary Completion (ANTICIPATED)
May 15, 2018
Study Completion (ANTICIPATED)
May 16, 2018
Study Registration Dates
First Submitted
February 3, 2018
First Submitted That Met QC Criteria
February 12, 2018
First Posted (ACTUAL)
February 19, 2018
Study Record Updates
Last Update Posted (ACTUAL)
April 4, 2018
Last Update Submitted That Met QC Criteria
April 3, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17-KAEK-178
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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