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PainvenipunctureNCT03437096

Postoperative Pain and Venipuncture Pain

A study testing venipuncture pain in people with Pain, run by Tokat Gaziosmanpasa University at 1 site in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Association between venipuncture pain and postoperative pain Read more about this study

Who is it for?
Ages 18 to 80 yearsHealthy volunteers can take part
Conditions the study is for
Pain
What is being tested?
venipuncture pain
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Jan 2018to 16 May 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • sleeve gastrectomy

Who cannot join

  • psychotic illness

Trial locations and contacts

1 site in 1 country.

Fatih Altiparmak, MD contact

03562320537

dr_altiparmak@hotmail.com

Fatih Altiparmak contact

03562320537

dr_altiparmak@hotmail.com

Turkey (Türkiye)1 site, 1 recruiting
  • Gaziosmanpasa University

    Tokat Province

    Mustafa Süren, MD

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: Association Between Postoperative Pain and Venipuncture Pain in Sleeve Gastrectomy Patients

Association between venipuncture pain and postoperative pain

Read the detailed description

Association will be find between venipuncture pain and postoperative pain in sleeve gastrectomy patients. Also we can study with pain catastrophising scale.

Conditions
Pain
Being tested
venipuncture pain
Medical subject headings
Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • venipuncture painOther

    postoperative sleeve gastrectomy patients pain

Study groups in NCT03437096
Study groupRoleWhat they receive
venipuncture painOtherpain during venipuncture
Receives: Other: venipuncture pain

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. numeric rating scale

    pain intensity 0 to 10 during venipuncture

    Measured: 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Feb 2018
  2. Study start15 Jan 2018
  3. Primary completion15 May 2018 (estimated)
  4. Study completion16 May 2018 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
1 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03437096
Sponsor's protocol ID
17-KAEK-178
Acronym
venipuncture
Status last verified
Apr 2018
First submitted
3 Feb 2018
Last updated
4 Apr 2018
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing venipuncture pain in people with Pain, run by Tokat Gaziosmanpasa University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 4 Apr 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Fatih Altiparmak, MD (03562320537, dr_altiparmak@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

numeric rating scale (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Apr 2018.

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