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Pecs II Block vs Surgical Infiltration for Postoperative Pain in Tendinopathy
Study Summary
This trial looks at two ways to control pain after surgery, and whether one is better than the other at reducing pain and the need for pain medication.
- Tendonitis
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You have significant liver or kidney problems, heart disease or congestive heart failure.You are allergic to oxycodone.You have been taking opioids to manage chronic pain for 3 months or more.You have been diagnosed or have reported problems with thinking or memory.You have a history of drug or alcohol abuse.You have had a neurological disorder in the past that affects how you feel pain.You are having shoulder surgery that includes a procedure called open subpectoral biceps tenodesis.
- Group 1: Pecs II block
- Group 2: Surgical infiltration
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
What is the participant enrollment size of this investigation?
"Affirmative. The online resource clinicaltrials.gov indicates that this research project, first posted on July 14th 2021, is actively recruiting participants. 160 patients need to be identified from a single medical site."
What qualifications are needed to participate in this research project?
"This clinical research is seeking 160 individuals with tendonitis, aged 18-75. To quality for the study, prospective participants must be within this age range and have already undergone shoulder arthroscopy with open subpectoral biceps tenodesis."
Does this trial cater to participants younger than thirty years of age?
"This clinical trial has set a lower age limitation of 18 and an upper limit of 75 for patient enrollment, in compliance with the stated criteria."
Are participants currently being recruited for this research project?
"Affirmative. Clinicaltrials.gov's records indicate that this trial is currently recruiting participants, having been first posted on July 14th 2021 and recently updated on June 14th 2022. The study aims to include 160 patients from a single site of research."
What potential harms could result from a Pecs II block procedure?
"Our team has assigned Pecs II block a score of 3, as it is in its fourth phase and thus already approved for use."
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