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OpenTrials
Completed

NCT Number: NCT03205852

Patients Decision-making in Rotator Cuff Surgery

The objective of this study was to evaluate the effect on patient treatment decision-making if information was given based on the benefit or on the side effect in rotator cuff disorders.

Completed

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients diagnosed with rotator cuff tears at their first clinical visit

Exclusion criteria

  • patients with a previous shoulder surgery, patients with worker's compensation and patients who were unwilling to participate and thereby not sign informed consent

Treatment and study plan

Questionnaire

Other

fulfillment of questionnaire

Primary outcomes

  1. questionnaire of surgery decision

    Time frame: immediate

    two proposals for surgery based on information given to the patient

Secondary outcomes

  1. Constant Score

    Time frame: immediate

    functional evaluation of shoulder function

Sponsors and collaborators

Lead sponsor

Hospital del Mar

Other

Registry information

Official study title

Do we Really Allow Patient Decision-making in Rotator Cuff Surgery? A Prospective Randomized Study

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Jul 2, 2017
Registry last updated
Jul 2, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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