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Pain, Chest clinical trials

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NCT ID: NCT06243718 Recruiting - Clinical trials for Diaphragmatic Paralysis

Phrenic Nerve Reconstruction for the Treatment of Diaphragmatic Paralysis: Patient Experiences and Reported Outcomes.

Start date: October 10, 2023
Phase:
Study type: Observational

This study utilizes a grounded theory methodology to explore patient experiences of phrenic nerve reconstructive surgery as a treatment for diaphragmatic paralysis.

NCT ID: NCT06222320 Not yet recruiting - Rib Fractures Clinical Trials

Kinesiotaping Method for Rib Fractures

Start date: April 1, 2024
Phase: Phase 2/Phase 3
Study type: Interventional

Kinesiotaping is used as a physiotherapy method to reduce muscle pain. In this technique, kinesiotaping tapes are attached to the relevant parts of the body. Patients experience serious pain in rib fractures. Kinesiotaping technique can potentially reduce pain by contributing to external stabilization of the ribs. In this study, patients with isolated rib fractures will be divided into two groups. The first group will be treated with kinesiotaping technique and routine painkillers. The second group will receive routine painkiller treatment. Pain scores between both groups will be compared.

NCT ID: NCT05283980 Active, not recruiting - Pain Clinical Trials

Pectoral Nerve Blocks (PECs) for Cardiovascular Implantable Electronic Device Placement

Start date: November 17, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether administration of a pectoral nerve blocks (Pecs I and II) with 0.25% bupivacaine are more effective as compared to placebo to provide analgesia for cardiac implantable electronic device (CIED) placement in cardiac electrophysiology lab

NCT ID: NCT05204043 Not yet recruiting - Pain Clinical Trials

Peter Hess® Sound Massage for Reducing Anxiety and Pain in Cardiac Surgery

MuSoCa
Start date: January 2022
Phase: N/A
Study type: Interventional

Cardiac surgery patients often undergo anxiousness and pain. Before surgery, anxiety is often caused by the idea of sternotomy, extracorporeal circulation, fear of post-operative pain, and even death. After surgery anxiety and pain can be the consequences of operative and peri-operative procedures. The investigators believe that reducing stress and pain by a relaxation therapy would lead to better stay in hospital and a better recovery after surgery. Music Care® relaxation technique consists into listening to an audio relaxing soundtrack chosen by the patient. This technique has already proven with several clinical studies its efficiency for reducing pain and anxiety in hospital. The research consists of comparing this technique to Peter Hess® sound massage for reducing pain and anxiety. The Peter Hess® sound massage is a holistic relaxation technique that uses sound vibrations generated by therapeutic singing bowls. Patients will be randomized in one of the two groups (Music Care® or Peter Hess®).

NCT ID: NCT04715932 Completed - Pain Clinical Trials

Study of Hesperidin Therapy on COVID-19 Symptoms (HESPERIDIN)

Hesperidin
Start date: February 18, 2021
Phase: Phase 2
Study type: Interventional

The main aim of this study is to determine the effects of short-term treatment with hesperidin on COVID-19 symptoms in comparison with a placebo. Treatment effects will be observed through a symptoms diary that will be completed by participants throughout the study and by taking the oral temperature daily.

NCT ID: NCT04134637 Completed - Pain, Chest Clinical Trials

Bilateral Pecto Intercostal Fascial Plane Block After Open Heart Surgeries

PIFB
Start date: October 1, 2019
Phase: N/A
Study type: Interventional

The objective is to test the effect of pecto intercostal fascial plane block (PIFB) as regard its impact on pain after sternotomy involved open heart surgery. The authors hypothesize that bilateral PIFB can reduce pain resulting from sternotomy following open heart surgeries.

NCT ID: NCT04094532 Completed - Pain, Acute Clinical Trials

Transversus Thoracic Muscle Plane Block for Open Heart Surgery

TTMP
Start date: October 1, 2019
Phase: N/A
Study type: Interventional

Poststernotomy pain is a complication of cardiac surgery. Poorly controlled pain is associated with myocardial ischemia, cardiac arrhythmias, hypercoagulability, pulmonary complications, and increased rates of delirium and wound infection. The transverse thoracic muscle plane (TTMP) block is a novel plane block that provide pain for sternotomy. The aim of this study was to evaluate the analgesic effect of ultrasound guided TTMP block in patients undergoing open heart surgery.

NCT ID: NCT04080934 Recruiting - Pain, Postoperative Clinical Trials

Breaststroke Swimming After Breast Cancer Treatment/Surgery as a Means of Treatment for Seroma, Lymphedema, and Chronic Arm and Chest Pain

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

Following surgery and treatment for breast cancer, many patients experience swelling of lymph nodes (lymphedema) or accumulation of fluid (seroma) that can cause pain, restrict movement, and reduce quality of life. Current treatments include massage, pressure dressings, and drainage, but these are often ineffective and do not last. Physical activity, in particular swimming, has been linked to improvement in lymphedema/seroma symptoms, but more research is required to determine whether or not this type of treatment is effective.

NCT ID: NCT03961048 Withdrawn - Pain, Postoperative Clinical Trials

Ideal Initial Bolus and Infusion Rate for Erector Spinae Plane Block Catheters

Start date: July 23, 2019
Phase: Phase 4
Study type: Interventional

This study would like to identify the best starting dose and infusion rate for nerve blocks and nerve catheters related to the erector spinae plane block that can improve functional status and pain control on cardiac surgery patients and minimize the necessity for opioid pain control using a continuous reassessment model.

NCT ID: NCT03874806 Withdrawn - Pain, Postoperative Clinical Trials

Pharmacokinetic Profile and Dermatomal Coverage of the Erector Spinae Plane Block

Start date: July 1, 2019
Phase: Phase 4
Study type: Interventional

The goals of this study are as follows: 1. to confirm the safe dosing of ropivacaine for the erector spinae plane block 2. develop a pharmacokinetic profile of the erector spinae plane block, which will help demonstrate how quickly and how closely toxic levels are reached when a routine dose of ropivacaine is given for this nerve block 3. assess numbness created by the erector spinae block when routine doses are administered