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Neuropathic Peripheral PainNCT06925256

Considering Peripheral Nerve Injury, Is It Safe to Perform Transradial Angiography?

A study testing nerve conduction study in people with Neuropathic Peripheral Pain, run by Bursa City Hospital.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

So far, apart from a limited number of case reports and small-scale studies, the frequency and severity of this complication have not been objectively evaluated using electromyography (EMG). Read more about this study

Who is it for?
Ages 20 to 60 years
Conditions the study is for
Neuropathic Peripheral Pain
What is being tested?
nerve conduction study
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
No sites listed yet
Study dates
1 Apr 2026to 30 Apr 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

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 20 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 20-60 years old patiens who applied trans angiograhy were included to study

Who cannot join

  • Having cognitive disorders
  • Patients who have story of cardiac pace / ICD,
  • History of polyneuropathy,
  • Previous nerve damages,
  • Deformities on arm,
  • Plexopathy,
Show all 10Show fewer
  • Radiculopathy,
  • Spinal surgery.
  • Having medical treatment for any kind of neuropathy
  • Having Cognitive disorders

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Taner Dandinoglu, MD. contact

90 533 691 4066

dandinoglu@gmail.com

Selma Kızıltoprak, MD. contact

90 534 855 6211

selmasimsek1996@gmail.com

About this study

Official title: Considerin Peripheral Nerve Injury, Is It Safe to Perform Transradial Angiography?

So far, apart from a limited number of case reports and small-scale studies, the frequency and severity of this complication have not been objectively evaluated using electromyography (EMG). In this study, presence, severity, and extent of nerve injury (one of the potential complications following the transradial approach (TRA)) were evaluated by EMG studies in patients managed at Bursa City Hospital.

Read the detailed description

Evaluation of peripheral nerve injury after transradial angiography with nerve conduction studies.

Being tested
nerve conduction study
Keywords
Nerve Conduction Studies, Nerve damage, Transradial angiography

What participants receive

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

  • nerve conduction studyDiagnostic test

    median ulnar and radial motor- sensory nerve conduction studies will be performed.

Study groups in NCT06925256
Study groupRoleWhat they receive
Patients with transradial angiographyExperimentalall patients involved evaluated with NCS
Receives: Diagnostic Test: nerve conduction study

What is being measured

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

  1. Nerve conduction studies (NCS)

    NCS (Nerve conduction study) findings obtained after radial intervention A NCS test measures how fast an electrical impulse moves through your nerve. NCS can identify nerve damage. During the test, your nerve is stimulated, often with electrode patches put on your skin. Two electrodes are placed on the skin over your nerve or over a muscle. One electrode stimulates your nerve with a very mild electrical impulse. The other electrode records it. The resulting electrical activity is recorded by another electrode. This is repeated for each nerve being tested. After test below values are obtained;

    • Velocity (meter/second),
    • Action potential amplitude (miliVolt)
    • Onset latans (milisecond)

    Measured: 1 day

Timeline

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

  1. First posted13 Apr 2025
  2. Study start1 Apr 2026 (estimated)
  3. Primary completion1 Apr 2027 (estimated)
  4. Study completion30 Apr 2027 (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
Screening
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06925256
Sponsor's protocol ID
2025-PMR-1
Status last verified
Feb 2026
First submitted
25 Mar 2025
Last updated
4 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: upon reasonable request will be provided by the authors

Questions about this trial

What is this clinical trial studying?

A study testing nerve conduction study in people with Neuropathic Peripheral Pain, run by Bursa City Hospital.

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 10 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: opening soon, as of the sponsor's last update on 4 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

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?

This study is still under way. Results are not available in the source record yet.

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

Contact Taner Dandinoglu, MD. (90 533 691 4066, dandinoglu@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Nerve conduction studies (NCS) (time frame: 1 day). 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 Feb 2026.

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