Soreness After Deep Dry Needling of One Latent Myofascial Trigger Point
1 other identifier
observational
60
0 countries
N/A
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 pain and sensitivity will be assessed during a 72 hours follow up period. Factors that may contribute to higher levels of pain or sensitivity will be evaluated.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2014
CompletedFirst Submitted
Initial submission to the registry
June 5, 2014
CompletedFirst Posted
Study publicly available on registry
June 6, 2014
CompletedJune 6, 2014
January 1, 2014
4 months
June 5, 2014
June 5, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
Pain
Visual analogue scale
72 hours
Secondary Outcomes (1)
Sensitivity
72 hours
Study Arms (1)
Latent trigger point in the upper trapezius muscle
Interventions
Eligibility Criteria
Healthy subjetct. Community sample from university.
You may qualify if:
- The latent MTrP diagnosis was based upon the following criteria:10
- presence of a palpable taut band in the muscle
- presence of a hypersensitive tender spot in the taut band
- palpable or visible local twitch response with snapping palpation of the tout band
- referred pain elicitation in response to compression.
You may not qualify if:
- presence of coagulation disorders
- neck or facial pain
- previous application of a dry needling technique
- MTrP therapy in head or neck within the previous 3 months
- fibromyalgia
- an insurmountable fear of needles as a reason of refusing the treatment
- history of surgery in the head or neck area.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 5, 2014
First Posted
June 6, 2014
Study Start
October 1, 2013
Primary Completion
February 1, 2014
Last Updated
June 6, 2014
Record last verified: 2014-01