Clavicle Splint for Pain Reduction After Posterior Cervicothoracic Surgery

NCT01977690 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2017-08-21

Study results available
· View outcomes & findings →

Summary

The purpose of the study is to see whether a clavicle splint can decrease the pain after posterior cervicothoracic surgery. The term "cervicle splint" conveys that the investigators do not deal with clavicle fractures here but use the splint he stabilize the posterior cervical area. The investigators want to demonstrate this in a prospective randomized manner.

Conditions

  • Posterior Cervical Surgery
  • Posterior Cervical Fusion
  • Posterior Cervical Laminectomy
  • Posterior Cervical Laminoplasty

Interventions

DEVICE

Clavicle Brace

Sponsors & Collaborators

Principal Investigators

  • Stephan Duetzmann · Stanford University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
95 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2014-08-31
Completion
2014-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01977690 on ClinicalTrials.gov