Recruiting NA Osteoarthritis Shoulder

New treatment option for Osteoarthritis Shoulder

Official title Diaphragm-Sparing Regional Anesthesia Techniques for Shoulder Surgery

ClinicalTrials.gov ID: NCT07474896

What this study is testing

What is Ropivacaine 0.2% for Interscalene Block?

Ropivacaine 0.2% for Interscalene Block is an investigational medicine, given as an injectable medicine, being studied as a potential treatment for osteoarthritis shoulder.

Also referred to as interscalene brachial plexus block.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
This study will compare two regional anesthesia techniques for shoulder surgery and evaluate their effects on diaphragmatic function. The standard regional anesthesia technique for shoulder surgery is the interscalene brachial plexus block (ISB), which provides effective analgesia but is frequently associated with ipsilateral hemidiaphragmatic paresis due to phrenic nerve involvement.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 65 to 100

You may be able to join if

  • Age ≥ 65 years
  • Elective shoulder surgery
  • ASA I-III
  • Planned use of regional anesthesia
  • Signed written informed consent

You likely can't join if

  • Allergy to local anesthetics
  • Planned continuous catheter technique
  • BMI \>40 kg/m²
  • Coagulopathy or anticoagulation
  • Pre-existing phrenic nerve palsy
  • Neurological disorder of the operative limb
See the full eligibility criteria
Who can join
  • Age ≥ 65 years
  • Elective shoulder surgery
  • ASA I-III
  • Planned use of regional anesthesia
  • Signed written informed consent
What rules you out
  • Allergy to local anesthetics
  • Planned continuous catheter technique
  • BMI \>40 kg/m²
  • Coagulopathy or anticoagulation
  • Pre-existing phrenic nerve palsy
  • Neurological disorder of the operative limb
  • Pregnancy or breastfeeding
  • Participation in another clinical trial within 30 days

The study team makes the final eligibility decision.

Where it's taking place

  • Poznan, Poland

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 65 years to 100 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Poznan, Poland. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.