NCT03499158

Brief Summary

Terminal latency index, residual latency and median ulnar F latency difference in carpal tunnel syndrome are specific parameters for the diagnosis

Trial Health

100
On Track

Trial Health Score

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

Enrollment
160

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2016

Shorter than P25 for all trials

Status
completed

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 1, 2016

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2016

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 2, 2016

Completed
2.1 years until next milestone

First Submitted

Initial submission to the registry

April 11, 2018

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 17, 2018

Completed
Last Updated

April 17, 2018

Status Verified

April 1, 2018

Enrollment Period

2 months

First QC Date

April 11, 2018

Last Update Submit

April 13, 2018

Conditions

Carpal Tunnel Syndrome

Outcome Measures

Primary Outcomes (1)

  • nerve conduction studies

    one month

Study Arms (2)

1

affected arms of patients who had gone to electrodiagnostic study and diagnosed as carpal tunnel syndrome

Other: nerve conduction study

2

healthy arms of patients who had gone to electrodiagnostic study and diagnosed as carpal tunnel syndrome in the other arms

Other: nerve conduction study

Interventions

nerve conduction studyOTHER

nerve conduction study

12

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients who had gone to electrodiagnostic study and diagnosed as carpal tunnel syndrome

You may qualify if:

  • Patients who had gone to electrodiagnostic study and diagnosed as carpal tunnel syndrome

You may not qualify if:

  • any history of hereditary polyneuropathies
  • acquired polyneuropathies
  • surgery or local steroid injections for upper limbs or effect the study
  • any history of fracture at the sites of stimulation or recording

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Carpal Tunnel Syndrome

Condition Hierarchy (Ancestors)

Median NeuropathyMononeuropathiesPeripheral Nervous System DiseasesNeuromuscular DiseasesNervous System DiseasesNerve Compression SyndromesCumulative Trauma DisordersSprains and StrainsWounds and Injuries

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Ufuk University

Study Record Dates

First Submitted

April 11, 2018

First Posted

April 17, 2018

Study Start

January 1, 2016

Primary Completion

March 1, 2016

Study Completion

March 2, 2016

Last Updated

April 17, 2018

Record last verified: 2018-04

Data Sharing

IPD Sharing
Will not share