Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2006-11-30
2009-12-31
Brief Summary
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Detailed Description
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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
Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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single-arm studies
Manual therapy for one group
Manual therapy
Manual therapy, once a week for 8 weeks
Interventions
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Manual therapy
Manual therapy, once a week for 8 weeks
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* heart block
* coagulopathy
* cognitive alterations and infection at the site
* patients using anticoagulants, and pregnant women
18 Years
60 Years
ALL
No
Sponsors
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Federal University of São Paulo
OTHER
Responsible Party
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Universidade Federal de São Paulo
Principal Investigators
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Rioko K Sakata, PhD
Role: STUDY_DIRECTOR
Universidade Federal de São Paulo
Locations
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Setor de Dor
São Paulo, São Paulo, Brazil
Countries
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Other Identifiers
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1276
Identifier Type: -
Identifier Source: org_study_id
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