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NCT04941118

Myofascial Pain Syndrome and Dextrose Prolotherapy

Status unknown Phase 4 Last updated 21 July 2021
What this trial tests

Phase 4 trial testing Injection of dextrose, local anesthetic and saline to the myofascial trigger point in Efficacy of Dextrose Prolotherapy in Myofascial Pain Syndrome in 60 participants. Status unknown.

Timeline
15 July 2021
Primary endpoint
30 December 2021
31 December 2021

Quick facts

Lead sponsorMustafa Kemal University
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment60
Start date15 July 2021
Primary completion30 December 2021
Estimated completion31 December 2021
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Mustafa Kemal University

Who can join

Adults 20 to 50, female only, with Efficacy of Dextrose Prolotherapy in Myofascial Pain Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Myofascial pain syndrome is characterized by the presence of hypersensitive points called trigger points that cause pain, tenderness, spasm, stiffness, limitation of movement, weakness, taut band within the muscle, and pain reflected by pressing in a muscle group or a single muscle. Prolotherapy is a regenerative treatment method in the treatment of chronic musculoskeletal pain, in which an irritating solution is injected, often hypertonic dextrose, into painful ligament and tendon attachments and adjacent joint spaces. In this study, it was aimed to examine the effect of prolotherapy application on pain, neck range of motion and neck disability in women with myofascial pain syndrome.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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