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临床试验/ACTRN12612000993897
ACTRN12612000993897已完成1 期

Randomised clinical trial to evaluate the effect of prolotherapy (Prt) injections and physiotherapy consisting of Mulligan's MWM and exercise (P/E) used singly and in combination, on pain and function in patients with lateral epicondylalgia (Tennis Elbow).

Griffith University0 个研究点目标入组 120 人开始时间: 2012年9月17日最近更新:

试验速览

阶段
1 期
状态
已完成
入组人数
120

研究概览

简要总结

ABSTRACT Objective: Lateral epicondylalgia (LE, tennis elbow) is a common, debilitating and often treatment-resistant condition. Two treatments thought to address the pathology of LE are hypertonic glucose plus lignocaine injections (prolotherapy) and a physical therapist guided manual therapy/exercise program (PT). This trial aimed to compare the short- and long-term clinical effectiveness, cost effectiveness, and safety of prolotherapy used singly and in combination with PT. Design: Single-blinded randomized clinical trial. Methods: 120 participants with LE of at least six weeks’ duration were randomly assigned to prolotherapy (4 sessions, monthly intervals), PT (weekly for 4 sessions) or combined (prolotherapy+PT). Patient-Rated Tennis Elbow Evaluation (PRTEE) and participant global impression of change scores were assessed by blinded evaluators at baseline, 6, 12, 26 and 52 weeks. Success rate was defined as the percentage of participants indicating elbow condition was either 'much improved' or 'completely recovered.’ Analysis was by intention-to-treat. Results: 88% completed the 12-month assessment. At 52 weeks, there were substantial, significant improvements compared with baseline status for all outcomes and groups, but no significant differences between groups. The PT group exhibited greater reductions in PRTEE at 6 and 12 weeks than the prolotherapy group. Duration of illness of less than 6 months predicted success rate, regardless of treatment. Conclusions: Pain and function measures improved substantially in all groups, more quickly in the PT group than prolotherapy group. The addition of prolotherapy to PT did not influence the rate of recovery.

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 60 Years(—)
性别
All

入选标准

  • Unilateral lateral elbow pain over the lateral epicondyle of at least 6 weeks duration which is aggravated by gripping, resisted wrist/finger extension and palpation, reduced pain-free grip force, as well as a minimum pain severity of 30 on a 0-100 mm visual analogue scale.

排除标准

  • Current pregnancy or breast feeding; presence of peripheral nerve involvement or cervical radiculopathy; systemic disorders including diabetes, rheumatoid arthritis or bleeding disorders; concomitant neck or other arm pain preventing usual work or recreation or necessitated treatment within the last 3 months; evidence of other primary sources of lateral elbow pain including osteoarthritis; sensory disturbance in the affected hand; history of upper limb dislocations, fractures or tendon ruptures within the preceding 10 years; allergy to corn, maize, or seafood; history of corticosteroid injection to the affected elbow within the previous 3 months; history of elbow surgery, malignancy or any medical condition which may contraindicate any of the study treatments; or unresolved litigation.

研究者

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