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The Specificity of Cervical Facet Medial Branch Blocks

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Johns Hopkins University

Status

Completed

Conditions

Cervical Facet Arthropathy
Neck Pain

Treatments

Procedure: Cervical medial branch blocks

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT00613340
NA-20008-A

Details and patient eligibility

About

Cervical facet arthropathy is a common cause of chronic neck pain. The "gold standard" for diagnosis is either blocking the facet joints, or more commonly blocking the medial branch nerves that innervate the joints. However, many studies have found a high false-positive rate when the nerves are blocked using 0.5 ml of local anesthetic. We will randomize patients to receive either cervical facet medial branch blocks with 0.25 ml of local anesthetic and contrast, or 0.5 ml. We will then do a CT scan to determine the accuracy and specificity of each block. Our hypothesis is that using the higher volume (0.5 ml) might be responsible for the high false-positive rate.

Full description

Inclusion criteria: Dept. of Defense beneficiaries > 18 years of age; neck pain > 3 months duration; cervical paraspinal tenderness Exclusion criteria: Radicular signs or symptoms; use of anticoagulants or bleeding disorder.

Outcome measures: The number of blocks whereby the contrast bathes the target nerve; the number of blocks whereby the contrast spreads to the medial branch nerve at the adjacent spinal level; the number of times the contrast diffuses into the intervertebral foramen or epidural space. We will also compare pain relief over 8 hours following the block between both volumes.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years
  • Chronic neck pain > 3 months
  • Paraspinal tenderness

Exclusion criteria

  • Absence of radicular symptoms
  • No bleeding diathesis
  • Contrast allergy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

1
Experimental group
Description:
Cervical medial branch blocks with 0.25 ml of injectate
Treatment:
Procedure: Cervical medial branch blocks
Procedure: Cervical medial branch blocks
2
Experimental group
Description:
Cervical medial branch blocks with 0.5 ml of local anesthetic and contrast
Treatment:
Procedure: Cervical medial branch blocks
Procedure: Cervical medial branch blocks

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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