ClinicalTrials.Veeva

Menu

Effect of Tourniquet on Sensory Nerve Conduction Threshold (sNCT) and OxyNeuroGram (ONG) Index- A Volunteer Study

Duke University logo

Duke University

Status

Completed

Conditions

Oxyneurogram Index
Sensory Nerve Conduction

Treatments

Device: tourniquet, sensory nerve conduction abnormality

Study type

Interventional

Funder types

Other

Identifiers

NCT01970839
Pro00048542

Details and patient eligibility

About

There are a number of risk factors for development of chronic pain that have been evaluated including age, gender, type and duration of surgery, duration of pain prior to surgery and tourniquet application. There is some scientific evidence from animal studies demonstrating that prolonged tourniquet application can result in lack of oxygen supply to nerves, and subsequent nerve damage resulting in chronic pain. This theory has not been proven in humans. In this study the investigators will indirectly assess the evidence for abnormalities caused by tourniquet application on subjects' nerves using well established devices to determine the function of these nerves.

Enrollment

10 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adults
  • Over 18 years of age

Exclusion criteria

  • Neurological disease
  • Diabetes mellitus
  • History of nerve injury
  • Chronic pain
  • Alcoholism
  • Blood pressure measurements greater than 140/80 and infection in the monitored area

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Tourniquet, pain, nerve injury, sensory nerve function
Other group
Treatment:
Device: tourniquet, sensory nerve conduction abnormality

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems