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Laser CO2 Versus TENS After Reconstruction of the Rotator Cuff

I

Istituto Ortopedico Rizzoli

Status

Completed

Conditions

Rotator Cuff Injury

Treatments

Procedure: LASER CO2
Procedure: TENS

Study type

Interventional

Funder types

Other

Identifiers

NCT01391000
0013483

Details and patient eligibility

About

The purpose of this study is to evaluate the most effective method between Transcutaneous Electrical Stimulation and Light Amplification by Stimulated Emission of Radiation therapy carbon dioxide therapy for pain control in the post-surgical rehabilitation of patients treated with reconstruction of the rotator cuff.

Full description

To evaluate the most effective method between Transcutaneous Electrical Stimulation and Light Amplification by Stimulated Emission of Radiation therapy carbon dioxide for pain control in the post-surgical rehabilitation of patients treated with reconstruction of the rotator cuff and to evaluate, at the end of the rehabilitation period, the range of motion, the function gained and the quality of life comparatively in the two groups of patients treated with Transcutaneous Electrical Stimulation or Light Amplification by Stimulated Emission of Radiation therapy carbon dioxide therapy.

Enrollment

70 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • subjects after surgery for rotator cuff injury of traumatic and / or degenerative

Exclusion criteria

  • concomitant fractures of the humerus, pace-maker, diseases for which treatments are contraindicated.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Laser CO2
Experimental group
Treatment:
Procedure: LASER CO2
TENS
Active Comparator group
Treatment:
Procedure: TENS

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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