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NCT05817578

Profiling the RCRSP Patient: a Pain Phenotype Classification Algorithm

Status unknown Last updated 22 June 2023
What this trial tests

trial testing Quantitative Sensory Testing / Dynamometry / Goniometry in Rotator Cuff Syndrome in 100 participants. Status unknown.

Timeline
2 September 2023
Primary endpoint
30 September 2024
30 September 2024

Quick facts

Lead sponsorUniversity of Thessaly
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment100
Start date2 September 2023
Primary completion30 September 2024
Estimated completion30 September 2024

Drugs / interventions tested

Conditions studied

Sponsor

University of Thessaly

Who can join

Adults 18 to 65, any sex, with Rotator Cuff Syndrome or Rotator Cuff Tears. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to collect a sum of different characteristics that have been mentioned previously in people presenting with RCRSP and by clustering them to create a phenotype system which may assist the individualisation of their management

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Rotator Cuff Syndrome

Currently open trials in the same condition.

Other University of Thessaly trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05817578.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing