DRKS00012859招募中2 期
Subacromial Pain Syndrome - the effects of a systematic osteopressure-treatment regarding pain and mobility - osteopressure with SAPS
FH Gesundheitsberufe OÖ0 个研究点目标入组 40 人开始时间: 2018年1月9日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 65 Years（—）
- 性别
- All
入选标准
- •For inclusion in study participation, points a) b) and c) must apply!
- •a) At least three of the six compulsory orthopedic stress tests are positive
- •b) The patient can repeatedly provoke pain by an active movement or by an active position (= functional DEMO)
- •c) At least ONE of the following diagnoses apply to the patient:
- •- Subacromial pain syndrome
- •- Periarthropathia humero-scapularis
- •- Unspecific shoulder pain (Dolores omi / Omalgie)
- •- Frozen Shoulder (primary and secondary)
- •- shoulder impingement syndrome, grade 1-3 (grade 3 only in partial rupture of the rotator cuff)
- •- Tendinitis of the rotator cuff
- •- Tendinitis calcarea of ??the rotator cuff
- •- Tendinitis of the long biceps tendon
- •- subacromial bursitis
- •- Bursitis calcarea subacromialis
- •- Partial ruptures of the rotator cuff
- •- Unspecific degeneration of the rotator cuff
排除标准
- •- Complete rupture of the rotator cuff (US or MRI or Arthro-MRI or arthroscopy confirmed)
- •- SLAP lesion type II / III / IV (Arthro-MRI or arthroscopy confirmed)
- •- Pulley lesion (US or MRI or Arthro-MRI or arthroscopically confirmed)
- •- Osteochondrosis of one or more joints of the shoulder complex
- •- osteoarthritis (from stage 2;
- •- Omarthritis (rheumatoid arthritis, purulent arthritis, tuberculous arthritis)
- •- humeral head nekrosis
- •- fractures of the bones involved in the shoulder complex less than 12 months ago
- •- Artificial joint replacement of one or more components of the glenohumeral joint
- •- Surgery on one or more joints or soft tissue structures of the shoulder complex less than 12 months ago
- •- Habitual shoulder dislocation
- •- status post shoulder luxation (event less than 6 months ago or more often than once dislocated)
- •- Tumor events in the body area to be treated (shoulder quadrant)
- •- advanced osteoporosis
- •- hemophilia
- •- fibromyalgia
- •- Not completely healed wounds in the treatment area (shoulder quadrant)
- •- Keloids in the treatment area (shoulder quadrant)
- •- neurological / neuromuscular / neuropsychological underlying disease or neuropathological event (central / radicular / peripheral nerve lesions)
- •- Acute or chronic mental illness, which possibly excludes a sane behavior of the subject or demonstrably favors a self- or foreign-endangering behavior
- •- insufficient verbal communication - e.g. because of linguistic barriers - between proband and therapist
- •- Limitations of mental functions that make participation in the study significantly more difficult
- •- Oral use or other administration of opioid painkillers, which can not be discontinued at least 7 days before the start of the study, OR is not expected to be maintained throughout the study period (6-8 days) in the same (!) dosage and dosage form
- •- Other on-going therapies that are likely to be suspected to affect the disease being studied (all conventional and complementary therapies and treatments included) and that may not be terminated or suspended for the duration of the study at least one week prior to the beginning of the study (first appointment)
- •- Participation in another medical study within the last three months or during the study period of this study
- •Relative exclusion criteria:
- •- Ongoing blood thinning medication
- •--> Subjects are informed that some side effects (see Study-Specific Risks and Side Effects) may be more pronounced (for example, increased hematoma formation) when taking blood-thinning medications. Since no other severe health damage is to be expected from this, the test subjects can still participate in the study if they want to accept the higher risks
研究者
相似试验
已完成
不适用
What kind of patients with subacromial pain are likely to benefit from a specific exercises strategy: A Randomized Controlled TrialJPRN-UMIN000024591Konan Woman University100
已完成
不适用
Subacromial impingement syndrome and paiTopic: Primary Care Research Network for England, MusculoskeletalSubtopic: Not Assigned, Musculoskeletal (all Subtopics)Disease: Musculoskeletal, All DiseasesMusculoskeletal DiseasesSubacromial impingement syndromeISRCTN42399123Keele University (UK)256
招募中
不适用
Comparison of Manual Therapy Versus Radial Shock Waves in the Shoulder Pain TreatmentShoulder ImpingementShoulder PainNCT06587399University of Alcala88
已完成
不适用
SISTIM: Subacromial Impingement Syndrome: The Identification of etiologic Mechanisms will have a new acronym respectively, SuSy SuSy: Subacromial Impingement Syndrome: The Identification of etiologic Mechanismspainful arc syndromesubacromial pain syndrome10023213NL-OMON41430eids Universitair Medisch Centrum110
已完成
不适用
US-guided Percutaneous Electrolysis (EPE®) in Shoulder PainShoulder PainNCT02569281Universidad Rey Juan Carlos50