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UnknownNCT04201249

Mesotherapy In Lateral Epicondylitis

MILES STUDY - Mesotherapy In Lateral Epicondylitis, a Prospective Randomized Controlled Study

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
82 (estimated)
Sponsor
Hospital de Santa Maria, Portugal · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Investigate the short- and long-term efficacy and safety of intradermal NSAIDs and lidocaine (delivered through mesotherapy) for the treatment of LE comparing it with empty intradermal injections.

Conditions

Interventions

TypeNameDescription
DRUGPiroxicam, lidocainePatients will be randomized to 2 groups group A - mesotherapy with piroxicam (20mg/ml, 1ml) and lidocaine (1%, 1.5ml) (treatment arm); group group B - mesotherapy without piroxicam
DEVICEMesotherapy without drug administrationPatients will be randomized to 2 groups group A - mesotherapy with piroxicam (20mg/ml, 1ml) and lidocaine (1%, 1.5ml) (treatment arm); group group B - mesotherapy without piroxicam

Timeline

Start date
2019-12-01
Primary completion
2021-12-12
Completion
2021-12-12
First posted
2019-12-17
Last updated
2019-12-18

Locations

1 site across 1 country: Portugal

Source: ClinicalTrials.gov record NCT04201249. Inclusion in this directory is not an endorsement.

Mesotherapy In Lateral Epicondylitis (NCT04201249) · Clinical Trials Directory