Recruiting NA Rotator Cuff Repair

New treatment option for Rotator Cuff Repair

Official title Unexpected Positive Cultures in Rotator Cuff Revision Surgery

ClinicalTrials.gov ID: NCT06257979

What this study is testing

What it's testing
In the context of rotator cuff re-intervention, the impact of Unexpected Positive Cultures (UPC) is not documented, and their management has not been studied, particularly regarding indications for antibiotic therapy, which is currently not a consensus. A prospective interventional study will be implemented to compare the results of non-randomized patient samples, whether positive or negative, taken during rotator cuff re-intervention.
  • 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 18 and older

You may be able to join if

  • Patient, male or female, aged 18 or over
  • Patient requiring re- intervention for Rotator Ruff Revision Surgery for non-healing of the same tendons after a first intervention (delay \<2 years)
  • Patient requiring arthroscopy
  • Patient having had realized a MRI of the shoulder in the 6 previous months
  • Affiliate participant or beneficiary of a social security scheme

You likely can't join if

  • Patient with at least one clinical sign of infection (fever, redness)
  • Patient with a new distant rupture on a healed cuff (\> 3 years)
  • Patient with a history of shoulder surgery other than initial Rotator Ruff Surgery
  • Patient having received antibiotic treatment in the 2 weeks preceding inclusion
  • Participant in another research
  • Participant in a period of exclusion from another research still in progress at the time of inclusion
See the full eligibility criteria
Who can join
  • Patient, male or female, aged 18 or over
  • Patient requiring re- intervention for Rotator Ruff Revision Surgery for non-healing of the same tendons after a first intervention (delay \<2 years)
  • Patient requiring arthroscopy
  • Patient having had realized a MRI of the shoulder in the 6 previous months
  • Affiliate participant or beneficiary of a social security scheme
  • Participant having been informed and not having objected to the use of their data
What rules you out
  • Patient with at least one clinical sign of infection (fever, redness)
  • Patient with a new distant rupture on a healed cuff (\> 3 years)
  • Patient with a history of shoulder surgery other than initial Rotator Ruff Surgery
  • Patient having received antibiotic treatment in the 2 weeks preceding inclusion
  • Participant in another research
  • Participant in a period of exclusion from another research still in progress at the time of inclusion
  • Protected participant: an adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision
  • Pregnant, breastfeeding or parturient woman
  • Participant hospitalized without consent

The study team makes the final eligibility decision.

Where it's taking place

  • Beaumont, France
  • Caen, France
  • Essey-lès-Nancy, France
  • Lyon, France
  • Muret, France
  • Nice, France
  • Saint-Herblain, France
  • Strasbourg, France

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, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Beaumont, France; Caen, France; Essey-lès-Nancy, France; Lyon, France; Muret, France; Nice, France and 2 more location(s). 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.