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NCT03794505 Clinical Trial

Quality of Life and Pain With Infiltration or Suprascapular Nerve Block in Glenohumeral Arthirtis

Shoulder Arthritis Clinical Trial

Official title:
Health Related Quality of Life and Pain Managment Using Infiltration or Suprascapular Nerve Block Ultrasound Guided in Patients With Glenohumeral Arthirtis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03794505
Other study ID # F-2018-3401-056
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date April 1, 2018
Est. completion date August 30, 2018

Study information
Verified date January 2019
Source Instituto Mexicano del Seguro Social
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Efficacy in pain and health related quality of life of suprascapular nerve block ultrasound guided and glenohumeral infiltration in glenohumeral arthritis

Description:

To describe the efficacy in pain management and health related quality of life of suprascapular nerve block ultrasound guided and glenohumeral infiltration in patients with glenohumeral arthritis

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date August 30, 2018
Est. primary completion date August 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- IMSS affiliated

- Glenohumeral arthritis diagnosed

Exclusion Criteria:

- Previusly treatment for the same disease

- No follow up

- Dead

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Methylprednisolone Acetate
depo-medrol 40 mg
• Lidocaine 2% Injectable Solution
2ml of 2% lidocaine
• Ropivacaine HCl Inj 7.5 MG/ML
25 mg

Locations
Country Name City State
Mexico Department of Orthopedics, UMAE "Dr. Victorio de la Fuente Narváez" IMSS-UNAM. Ciudad de México, México Mexico City Gustavo A Madero

Sponsors (1)
Lead Sponsor Collaborator
Instituto Mexicano del Seguro Social

Country where clinical trial is conducted

Mexico, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain before visual analogue scale VAS before intervention
Primary Pain 2 months after Visual analogue scale 2 months after procedure VAS 2 months after
Primary Pain 6 months after Visual analogue scale 6 months after procedure VAS 6 months after
Secondary Quality of life before procedure SF12v2 Health related quality of life before procedure SF12v2 before procedure
Secondary Quality of life 2 months after procedure SF12v2 Health related quality of life 2 months after SF12v2 2 months after
Secondary Quality of life 6 months after procedure SF12v2 Health related quality of life 6 months after SF12v2 6 months after
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