NCT03842072 (C-PASS) is a NA clinical trial of Cervical collar in Cervical Radiculopathy, sponsored by Unity Health Toronto.

Who is sponsoring NCT03842072?

NCT03842072 is sponsored by Unity Health Toronto.

What drugs are being tested in NCT03842072?

Interventions in NCT03842072: Cervical collar.

What condition does NCT03842072 study?

NCT03842072 studies Cervical Radiculopathy, Cervical Myelopathy.

Is NCT03842072 still recruiting?

NCT03842072 is currently status unknown. Last updated 18 September 2019.

Last reviewed 2019-09-18 · How we verify

NCT03842072: C-PASS

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

The Collar Post Anterior Cervical Spine Surgery Study

Status unknown NA Last updated 18 September 2019

What this trial tests

NA trial testing Cervical collar in Cervical Radiculopathy in 244 participants. Status unknown.

Timeline

23 February 2018

Primary endpoint
1 July 2020

1 July 2021

Quick facts

Lead sponsor	Unity Health Toronto
Phase	NA
Status	Status unknown
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	none
Primary purpose	treatment
Enrollment	244
Start date	23 February 2018
Primary completion	1 July 2020
Estimated completion	1 July 2021
Sites	2 locations across Canada

Drugs / interventions tested

Cervical collar

Conditions studied

Cervical Radiculopathy — all drugs for Cervical Radiculopathy →
Cervical Myelopathy — all drugs for Cervical Myelopathy →

Sponsor

Unity Health Toronto — full company profile →

Who can join

Adults 18 to 80, any sex, with Cervical Radiculopathy or Cervical Myelopathy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The Anterior Cervical Discectomy and Fusion (ACDF) represents one of the most commonly performed spinal operations internationally, often in the context of symptomatic radiculopathy or myelopathy secondary to cervical degenerative disease. Approximately half of surgeons continue to prescribe a period of post-operative bracing with a cervical collar. However, there is currently no high quality evidence available to support the routine use of post-operative bracing after ACDF; further, braces are expensive and have been associated with a variety of local complications. In summary, the current lack of evidence, and lack of consensus amongst surgeons, regarding best practices in the use of post-operative bracing after ACDF, places the surgeon and the patient in a precarious position. Our randomized trial comparing the impact of 6 weeks of post-operative bracing with a rigid cervical collar vs. no post-operative bracing, on a variety of clinical and radiological outcomes, for adult patients with cervical radiculopathy and/or myelopathy undergoing single or multi-level ACDF.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Cervical collar

Trials testing the same drug.

NCT03754270 — Cervical Collar for Patients With Moderate Obstructive Sleep Apnea · NA · completed
NCT04572113 — Comparison of Cervical Motion Restriction and Interface Pressure Between Two Cervical Collars · completed
NCT03400644 — Are Rigid Cervical Collars Necessary for Open-door Laminoplasty and Titanium Arch Plates for Cervical Myelopathy? · NA · completed

Other recruiting trials for Cervical Radiculopathy

Currently open trials in the same condition.

NCT07307846 — Investigation of the Effects of Interlaminar Epidural Steroid Injection on Upper Extremity Proprioception in Patients Wi · NA · recruiting
NCT07447271 — Ultrasound Guided Cervical Selective Nerve Root Block Versus Fluoroscopic Guided Cervical Transforaminal Epidural Block · NA · active not recruiting
NCT07319156 — Assessment of Upper Extremity Proprioception in Patients With Cervical Radiculopathy · recruiting
NCT07207356 — Ultrasound Guided Transcutaneous Pulsed Radiofrequency for Cervical Radiculopathy · NA · recruiting
NCT07365917 — Effect of Core Stabilization Exercises on Patients With Cervical Radiculopathy · NA · recruiting

Other Unity Health Toronto trials

Trials by the same sponsor.

NCT07507409 — Innovative Sternal Closure Techniques: Evaluating STRATAFIX™ and DERMABOND™ for Reduced Complications in CABG Patients · Phase 4 · not yet recruiting
NCT07455487 — First Appendectomy Using Revolve Surgical Robotic Arm · NA · not yet recruiting
NCT07301632 — Ecstasy to Alleviate SEvere Chronic Neuropathic Pain Trial · Phase 2 · recruiting
NCT07314905 — Adaptive Platform Trial of Treatments for Respiratory Infections in Community Settings (TreatResp) · Phase 3 · not yet recruiting
NCT06571916 — Brief Skills for Safer Living (Brief-SfSL) · NA · recruiting

Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT03842072 (US National Library of Medicine, public domain)
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Unity Health Toronto
Last refreshed: 18 September 2019

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03842072.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing