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

Status

Unknown

Conditions

Intervention / Treatment

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.

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

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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