NCT Number: NCT02158104
Soreness After Deep Dry Needling of One Latent Myofascial Trigger Point
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.
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Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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.
Exclusion criteria
- 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.
Treatment and study plan
Primary outcomes
-
Pain
Time frame: 72 hours
Visual analogue scale
Secondary outcomes
-
Sensitivity
Time frame: 72 hours
Pressure pain threshold
Sponsors and collaborators
Lead sponsor
CEU San Pablo University
Other
Registry information
Important dates
- Study start
- 2013
- Primary completion
- 2014
- First posted
- Jun 6, 2014
- Registry last updated
- Jun 6, 2014
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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View Trial Details