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Management of Popeye Sign With Botulinum Toxin After Bicepstenotomy

NCT04750291 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2021-10-22

No results posted yet for this study

Summary

Double-blinded randomized controlled trial with 20 people of whom 10 will receive a placebo infiltration and 10 an infiltration with botulinum toxin type A for cramping pain after arthroscopic tenotomy of the long head of the biceps tendon.

Conditions

  • Popeye Syndrome

Interventions

DRUG

Botulinum toxin type A

1 infiltration in the biceps muscle with botulinum toxin (100 IU)

OTHER

Placebo

1 infiltration in the biceps muscle with placebo or sterile saline

Sponsors & Collaborators

  • AZ Delta

    lead OTHER

Principal Investigators

  • Bert Vanmierlo, MD · Orthopedie Roeselare AZ Delta

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2021-08-09
Primary Completion
2022-12-31
Completion
2022-12-31

Countries

  • Belgium

Study Locations

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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 NCT04750291 on ClinicalTrials.gov