Post Dry Needling Soreness. Description and Treatment

This study is currently recruiting participants.

Verified May 2012 by CEU San Pablo University

Sponsor:

Information provided by (Responsible Party):

CEU San Pablo University

ClinicalTrials.gov Identifier:

NCT01608633

First received: May 27, 2012

Last updated: May 30, 2012

Last verified: May 2012

History of Changes

Tracking Information
First Received Date ^ICMJE	May 27, 2012
Last Updated Date	May 30, 2012
Start Date ^ICMJE	March 2012
Primary Completion Date	Not Provided
Current Primary Outcome Measures ^ICMJE (submitted: May 30, 2012)	Pain [ Time Frame: 72 hours ] [ Designated as safety issue: No ] Visual analogue scale
Original Primary Outcome Measures ^ICMJE	Same as current
Change History	Complete list of historical versions of study NCT01608633 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE (submitted: May 30, 2012)	Pain [ Time Frame: 48 hours ] [ Designated as safety issue: No ] Pressure pain threshold Psychological factors [ Designated as safety issue: No ] Symptom check list. SCL-90
Original Secondary Outcome Measures ^ICMJE	Same as current
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Post Dry Needling Soreness. Description and Treatment
Official Title ^ICMJE	Not Provided
Brief Summary	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.
Detailed Description	Not Provided
Study Type ^ICMJE	Interventional
Study Phase	Phase 2
Study Design ^ICMJE	Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single Blind (Investigator) Primary Purpose: Treatment
Condition ^ICMJE	Pain After Dry Needling
Intervention ^ICMJE	Other: Spray and stretch Physiotherapeutic technique which consist in stretching the muscle while a cold spray is applied on the skin.
Study Arm (s)	Experimental: Spray and stretch Intervention: Other: Spray and stretch No Intervention: Control
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Recruiting
Enrollment ^ICMJE	Not Provided
Completion Date	Not Provided
Primary Completion Date	Not Provided
Eligibility Criteria ^ICMJE	Inclusion Criteria: Subjects presenting latent trigger points in the trapezius muscle Exclusion Criteria: Subjects with active trigger points or absence of trigger points.
Gender	Both
Ages	18 Years to 65 Years
Accepts Healthy Volunteers	Yes
Contacts ^ICMJE	Not Provided
Location Countries ^ICMJE	Spain

Administrative Information
NCT Number ^ICMJE	NCT01608633
Other Study ID Numbers ^ICMJE	CEU-001
Has Data Monitoring Committee	Not Provided
Responsible Party	CEU San Pablo University
Study Sponsor ^ICMJE	CEU San Pablo University
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	CEU San Pablo University
Verification Date	May 2012
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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