- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01608633
Effects of Spray and Stretch on Postneedling Soreness and Sensitivity After Dry Needling of a Latent Myofascial Trigger Point.
September 3, 2013 updated by: CEU San Pablo University
Pain after dry needling or injection in the muscle is a frequent secondary effect in the treatment of myofascial pain syndrome.
In this trial spray and stretch technique is evaluated as a method to reduce this soreness.
As well, the characteristics and the different factors that influence in this pain will be described.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
70
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Madrid, Spain, 28668
- CEU San Pablo University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Subjects presenting latent trigger points in the trapezius muscle
Exclusion Criteria:
- Subjects with active trigger points or absence of trigger points.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control
|
|
Experimental: Spray and stretch
|
Physiotherapeutic technique which consist in stretching the muscle while a cold spray is applied on the skin.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain
Time Frame: 72 hours
|
Visual analogue scale
|
72 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain
Time Frame: 48 hours
|
Pressure pain threshold
|
48 hours
|
Psychological factors
Time Frame: 72 hours after needling
|
Symptom check list revised.
SCL-90-r
|
72 hours after needling
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2012
Primary Completion (Actual)
April 1, 2013
Study Registration Dates
First Submitted
May 27, 2012
First Submitted That Met QC Criteria
May 30, 2012
First Posted (Estimate)
May 31, 2012
Study Record Updates
Last Update Posted (Estimate)
September 4, 2013
Last Update Submitted That Met QC Criteria
September 3, 2013
Last Verified
September 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- CEU-001
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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