NCT03437096

Brief Summary

Association between venipuncture pain and postoperative pain

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1

participants targeted

Target at below P25 for not_applicable pain

Timeline
Completed

Started Jan 2018

Shorter than P25 for not_applicable pain

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 15, 2018

Completed
19 days until next milestone

First Submitted

Initial submission to the registry

February 3, 2018

Completed
16 days until next milestone

First Posted

Study publicly available on registry

February 19, 2018

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2018

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 16, 2018

Completed
Last Updated

April 4, 2018

Status Verified

April 1, 2018

Enrollment Period

4 months

First QC Date

February 3, 2018

Last Update Submit

April 3, 2018

Conditions

Pain

Outcome Measures

Primary Outcomes (1)

  • numeric rating scale

    pain intensity 0 to 10 during venipuncture

    3 months

Study Arms (1)

venipuncture pain

OTHER

pain during venipuncture

Other: venipuncture pain

Interventions

venipuncture painOTHER

postoperative sleeve gastrectomy patients pain

venipuncture pain

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • sleeve gastrectomy

You may not qualify if:

  • psychotic illness

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gaziosmanpasa University

Tokat Province, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Mustafa Süren

    Gaziosmanpasa University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Fatih Altiparmak, MD

CONTACT

03562320537dr_altiparmak@hotmail.com

Fatih Altiparmak

CONTACT

03562320537dr_altiparmak@hotmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Anesthesiology and reanimation

Study Record Dates

First Submitted

February 3, 2018

First Posted

February 19, 2018

Study Start

January 15, 2018

Primary Completion

May 15, 2018

Study Completion

May 16, 2018

Last Updated

April 4, 2018

Record last verified: 2018-04

Locations

TU(1)