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Shoulder Pain clinical trials

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NCT ID: NCT02558686 Completed - Shoulder Pain Clinical Trials

Exercise and Post-dry Needling Soreness

Start date: October 2015
Phase: N/A
Study type: Interventional

Application of trigger point dry needling can induce post-dry needling soreness. This is not a negative experience, but sometimes some patients want to reduce it as much as possible. Manual therapies and exercise strategies targeting to decrease post-dry needling soreness need to be investigated.

NCT ID: NCT02554968 Completed - Clinical trials for Head and Neck Cancer

Reliability and Validity of Patient Reported Outcome Measures in Head and Neck Cancer

Start date: September 2015
Phase:
Study type: Observational

This study will utilize Rasch analysis to study the construct validity and reliability of five shoulder-related patient-reported outcome measures in patients reporting shoulder impairment following surgery for head and neck cancer.

NCT ID: NCT02541448 Completed - Shoulder Pain Clinical Trials

Pneumoperitoneum Management With SurgiQuest AirSeal at Low vs. Higher Pressure ( PRESSURE )

PRESSURE
Start date: July 2015
Phase: N/A
Study type: Interventional

This study is designed to evaluate physician preference related to the use of the SURGIQUEST AIRSEAL® INSUFFLATION SYSTEM (AIS) at low verses high pressure for the management of pneumoperitoneum.

NCT ID: NCT02541279 Completed - Shoulder Pain Clinical Trials

Effectiveness of a Group Intervention for the Treatment of Shoulder Pathologies

Start date: November 2014
Phase: N/A
Study type: Interventional

The investigators determined the effectiveness of a group intervention for the treatment of shoulder pathologies.

NCT ID: NCT02517437 Completed - Shoulder Pain Clinical Trials

Suprascapular and Axillary Blocks Versus Interscalene Block for Shoulder Surgery

PASS
Start date: August 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the combination of suprascapular and axillary nerve blocks is non-inferior to the conventional interscalene block (ISB) in providing pain relief during the first postoperative day to adult healthy patients (age > 18) undergoing ambulatory shoulder surgery.

NCT ID: NCT02491489 Completed - Shoulder Pain Clinical Trials

Activity of the Rotator Cuff During Glenohumeral Mobilization

Start date: March 2015
Phase: N/A
Study type: Interventional

Shoulder pain is one of the most common musculoskeletal conditions treated by physical therapists. One common treatment is passive glenohumeral joint accessory mobilization, which is the application of a therapist generated force to move the humeral head (ball) on the glenoid (socket) of the shoulder to improve motion and decrease pain. It is generally accepted that these mobilizations do not elicit active muscular contractions of the surrounding musculature. However, there is very little literature to support this assumption, and a preliminary PubMed search utilizing the terms "shoulder"," mobilization", and "EMG" returned zero relevant references. Therefore, the investigators plan to utilize surface electromyography (EMG), a non-invasive assessment tool, to objectively measure the activity of the rotator cuff muscles (the muscles that surround the shoulder and provide stability to the joint) during various grades(levels of force and amplitude of movement) of glenohumeral mobilization ( a standard of care treatment). It is also unknown if subjects pain levels impact the level of rotator cuff activity. To investigate these questions, the investigators will collect EMG data while performing mobilizations on a total of 20 subjects, divided into two groups: 10 pain free shoulders and 10 painful shoulders. Data analysis will then include descriptive analysis, estimates of effect size, and analysis for between group differences. The investigators hypothesize that there will be significant differences in muscular activity between groups related to the presence of shoulder pain.

NCT ID: NCT02469961 Completed - Shoulder Pain Clinical Trials

Dexmedetomidine vs Propofol TIVA (Total Intravenous Anesthesia) and Interscalene Block

TIVA
Start date: October 2010
Phase: Phase 4
Study type: Interventional

The standard hospital procedure calls for the patient to undergo Interscalene block under ultrasound with or without nerve stimulation guidance prior to going to operating room (OR). The block utilizes a 40 ml mixture of 0.5% Ropivacaine and Lidocaine 1.5%. At this time the patient receives preliminary sedation with Midazolam 1mg IV and Fentanyl 50 mcg IV. The participant is then brought to the OR and prolonged sedation is initiated, randomly using either Dexmedetomidine or Propofol. The primary objective of the present study is to use Dexmedetomidine for sedation, and compare the outcomes with Propofol sedation. The investigators will enroll 50 patients for this study. Our hypothesis is that Dexmedetomidine will cause fewer episodes of intermittent apnea, and reduced need for supplemental medication for sedation, compared to Propofol

NCT ID: NCT02465853 Completed - Stroke Clinical Trials

Hemiplegic Shoulder Pain and Rotator Cuff Injuries

Start date: January 2015
Phase: N/A
Study type: Interventional

Hemiplegic shoulder pain (HSP) is one of most complications after stroke. HSP would impede rehabilitation programs and the motor recovery of affected upper extremity. HSP was associated with impaired daily life activities and prolong hospital stay after stroke. Therefore, effective managements is important in stroke patients with HSP. Rotator cuffs injuries are related to HSP. Clinically, hyaluronic acid (HA) is used for rotator cuff injuries. Previous researchers reported that HA could provide pain relief, improved motion, and increased daily activities. In this study, fifty subacute stoke patients will be enrolled. These patients will be allocated into group A and B randomly. The patients in group A received HA injection while patients in group B received normal saline injection. Patients from both groups received injection for 3 times each on the 1st, 2nd, 3rd week. All the patients will still receive rehabilitation programs of physical therapy and occupational therapy. Each patient will receive physical, sonographic examinations, and stroke Specific Quality of Life Scale (SSQOL). The aims of this study are to investigate the benefits of HA injection on pain relief, motor function recovery, and life quality in subacute stroke patients with HSP before and after HA injection.

NCT ID: NCT02449668 Completed - Shoulder Pain Clinical Trials

Acupuncture Treatment of Shoulder Impingement Syndrome

Start date: March 2012
Phase: N/A
Study type: Interventional

The main objective of the current study was to assess the analgesic effect achieved to short- and medium-term by the use of acupuncture on individuals with impingement syndrome of the shoulder, in comparison to the use of acupuncture at sham points. Furthermore, secondary objectives were also sought, such as the short- to medium-term functional recovery of the affected joint, knowing the possible influence that this has over the recovery of the laterality of the subject, as well as the development of a protocol to select points to treat pain affecting the shoulder area.

NCT ID: NCT02445599 Completed - Pain Clinical Trials

Diclofenac Premedication, as the Effect of Preemptive Analgesia After Post-thoracotomy Chest and Shoulder Pain

Start date: April 2014
Phase: Phase 4
Study type: Interventional

The purpose of the study is to examine if the hyposthesis of the preventive analgestic characteristic of diclofenac given preoperatively has any effect on postoperative thoracic wall and shoulder pain sensation. We also want to examine the rescue analgetic consumption and the postoperative lung function test values.