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NCT01381380 Clinical Trial

Manual Therapy Treatment for Myofascial Pain

Myofascial Pain Syndromes Clinical Trial

Official title:
Effect of Manual Therapy After Trigger Point Injection for Myofascial Pain Syndrome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01381380
Other study ID # 1276
Secondary ID
Status Completed
Phase N/A
First received June 23, 2011
Last updated June 24, 2011
Start date November 2006
Est. completion date December 2009

Study information
Verified date November 2007
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

This study is a pain intensity evaluation in patients with myofascial pain submitted kinesitherapy after trigger point injection.

Description:

Randomized prospective study conducted on 30 patients of both genders ranging in age from 18 to 60 years, with neck and shoulder girdle Myofascial Pain Syndrome (MFS), with a duration of ≥ 4 months and pain intensity ≥ 4.

Trigger point injection of 1 mL 0.25% bupivacaine at each point, once a week for 8 weeks (T1 to T8).

Group 1: kinesiotherapy once a week for 8 weeks Group 2: not submitted to kinesiotherapy Evaluation of pain intensity on the first assessment (T0) and after 1, 2, 3, 4, 5, 6, 7, 8, and 9 weeks

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date December 2009
Est. primary completion date November 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- myofascial pain of neck and shoulder girdle, lasting = 4 months, pain intensity = 4.

Exclusion Criteria:

- arrhythmia

- heart block

- coagulopathy

- cognitive alterations and infection at the site

- patients using anticoagulants, and pregnant women

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Manual therapy
Manual therapy, once a week for 8 weeks

Locations
Country Name City State
Brazil Setor de Dor São Paulo

Sponsors (1)
Lead Sponsor Collaborator
Federal University of São Paulo

Country where clinical trial is conducted

Brazil, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain intensity once a week for 8 weeks (T1 to T8) 8 weeks No
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