Clinical Trials for Chest Pain

Currently registered clinical trials for Chest Pain from ClinicalTrials.gov. 23 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Chest Pain from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 23
  • Active, not recruiting: 5
  • Completed: 12
  • Other: 10

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT00081523 — Natural History of Sickle Cell Disease

StatusRecruiting
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment3500
Study TypeOBSERVATIONAL
ConditionsPain Crisis

This study is not a treatment protocol and no experimental treatments are involved. Study participants may be seen as needed for clinical, translational and basic research studies, or as medically indicated. Subjects will receive their general medical care outside the NIH and will be seen at our clinic or at CNHS with varying frequency. Subjects may be seen for multiple visits. Subjects may be …

NCT02845531 — Implantable Cardioverter Defibrillator Versus Optimal Medical Therapy In Patients With Variant Angina Manifesting as Aborted Sudden Cardiac Death

StatusRecruiting
PhasePhase 4
SponsorKee-joon Choi
Enrollment140
Study TypeINTERVENTIONAL
ConditionsAngina Pectoris, Variant; Sudden Cardiac Death
Interventions;

The purpose of this study is to determine whether ICD(Implantable Cardioverter Defibrillator) implantation on the top of optimal medical therapy in patients with variant angina manifesting as aborted sudden cardiac death reduces the incidence of the death from any cause compared with optimal medical therapy alone.

NCT06295679 — A Study Assessing Repatha® in Combination With Standard of Care (SOC) Compared With SOC on Major Cardiovascular Events in Chinese Participants With Atherosclerotic Cardiovascular Disease

StatusRecruiting
PhaseN/A
SponsorAmgen
Enrollment7000
Study TypeOBSERVATIONAL
ConditionsMajor Cardiovascular Event; Established Atherosclerotic Cardiovascular Disease

The primary objective of the study is to evaluate real-world effectiveness of treatment with Repatha® in combination with SOC, compared with SOC alone, on the risk for cardiovascular (CV) death, myocardial infarction (MI), stroke, hospitalization for unstable angina, or coronary revascularization, whichever occurs first, in participants with established atherosclerotic CV disease (ASCVD) treate…

NCT07677540 — Continuous Erector Spinae Block Versus Thoracic Epidural Analgesia for the Prevention of Chronic Pain Following Thoracotomy: a Retrospective Study

StatusRecruiting
PhaseN/A
SponsorMeir Medical Center
Enrollment34
Study TypeOBSERVATIONAL
ConditionsThoracic Surgery
Interventions;

Post-thoracotomy pain syndrome (PTPS) is a prevalent complication that significantly impacts patients’ quality of life, with reported incidence ranging from 25% to 90%. This study evaluated the effectiveness of continuous erector spinae plane (ESP) block compared to thoracic epidural analgesia (TEA), the current gold standard, in preventing PTPS. Our goal was to compare the incidence of PTPS be…

NCT07290582 — Phrenic Infiltration as Cryoanalgesia Adjuvant for Early Postoperative Pain Following the Nuss Procedure

StatusRecruiting
PhaseN/A
SponsorPapa Giovanni XXIII Hospital
Enrollment50
Study TypeOBSERVATIONAL
ConditionsPectus Excavatum; Cryo Analgesia; Phrenic Nerve-related Diaphragmatic Impairment

The goal of this observational ambispective study is to compare the effectiveness of two pain management strategies in pediatric patients undergoing the Nuss procedure for pectus excavatum. The main questions it aims to answer are:

Does the addition of phrenic Infiltration as Cryo Adjuvant (PhICA) to earlier percutaneous intercostal cryoanalgesia (EPIC) reduce postoperative pain scores compare…

NCT05351229 — Intrathecal Morphine for Analgesia in Video-assisted and Robotic-assisted Thoracic Surgery

StatusRecruiting
PhasePhase 4
SponsorNorthwestern University
Enrollment90
Study TypeINTERVENTIONAL
ConditionsPain, Postoperative
Interventions;

VATS/RATS is widely used for diagnosis and treatment of intrathoracic conditions. Despite many benefits, postoperative pain continues to be intense after VATS/RATS. The optimal strategy for pain management has not been defined. In this randomized, placebo-controlled, double-blinded clinical investigation, investigators hypothesize that 5 mcg/kg intrathecal morphine will decrease postoperative a…

NCT06384846 — Diagnostic Performance of Artificial Intelligence Algorithms in Prediction of Acute Coronary Syndrome Based on White Blood Cell Properties

StatusRecruiting
PhaseN/A
SponsorRobotDreams GmbH
Enrollment3350
Study TypeOBSERVATIONAL
ConditionsAcute Coronary Syndrome; Angina Pectoris; NSTEMI - Non-ST Segment Elevation MI; STEMI - ST Elevation Myocardial Infarction; Unstable Angina (UA)

The goal of this observational study is to evaluate whether artificial intelligence (AI) algorithms can predict or exclude acute coronary syndrome (ACS) in adults using data generated by routine hematology testing. The main questions the study aims to answer are:

  • Can AI algorithms based on white blood cell (WBC) data predict or exclude ACS in subjects with suspected ACS?
  • Can erythrocyte (E…

NCT06239974 — Vericiguat in Patients With Coronary Microvascular Dysfunction Causing Stable Chest Pain (V-COM)

StatusRecruiting
PhaseN/A
SponsorThe University of Hong Kong
Enrollment94
Study TypeINTERVENTIONAL
ConditionsChest Pain
Interventions;

This is a randomised controlled trial to determine the effectiveness of Vericiguat to improve stress myocardial blood flow (MBF) and myocardial perfusion reserve as measured by cardiac magnetic resonance (CMR) imaging.

NCT07091682 — Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold System in the Treatment of Subjects With Long de Novo Lesions

StatusRecruiting
PhaseN/A
SponsorBiotronik AG
Enrollment100
Study TypeINTERVENTIONAL
ConditionsCoronary Artery Disease; Atherosclerosis of Coronary Artery; Myocardial Ischemia; Ischemic Heart Disease; Acute Coronary Syndromes
Interventions

The study objective is the assessment of safety and clinical performance of Freesolve 35- and 40-mm in de novo coronary artery lesions up to 38 mm length.

NCT07638137 — Advanced Invasive Diagnosis Strategy for Post-PCI Patients With Stable Coronary Syndromes Undergoing Coronary Angiography

StatusRecruiting
PhaseN/A
SponsorFundacion Investigacion Interhospitalaria Cardiovascular
Enrollment246
Study TypeOBSERVATIONAL
ConditionsAngina (Stable); Percutaneous Coronary Intervention (PCI); INOCA (Ischemia With Non Obstructive Coronary Artery Disease); Chronic Coronary Syndrome
Interventions

AID Post-PCI Angina is as an observational, prospective, single-cohort, multicenter study designed to investigate the causes and origins of post-PCI angina by using the advance invasive diagnosis (AID) strategy combining with angiography derived physiology (ADP) in an all-comers population of patients with post-PCI angina referred for invasive coronary angiography. An all-comers population of p…

NCT07657546 — MCG for Non-Obstructive Myocardial Ischemia

StatusRecruiting
PhaseN/A
SponsorQilu Hospital of Shandong University
Enrollment3786
Study TypeOBSERVATIONAL
ConditionsMyocardial Ischemia
Interventions

The aim of this prospective study is to identify Non-Obstructive Myocardial Ischemia of patients who have acute chest pain using Magnetocardiography.

NCT07027891 — The Rule-Out Acute Myocardial Infarction Using Aritifical Intelligence Electrocardiogram (ROMIAE) 2 Trial

StatusRecruiting
PhaseN/A
SponsorCHA University
Enrollment4670
Study TypeINTERVENTIONAL
ConditionsMyocardial Infarction (MI); Chest Pain Rule Out Myocardial Infarction
Interventions

This study is to see whether the AI ECG assisted protocol is as safe and efficacious as conventional protocol in early triage of suspected myocardial infarction.

NCT07123181 — Oregano and Basil Leaves and Coronary Artery Disease

StatusRecruiting
PhaseN/A
SponsorShahid Beheshti University of Medical Sciences
Enrollment70
Study TypeINTERVENTIONAL
ConditionsAcute Coronary Syndromes; Unstable Angina (UA)
Interventions;

The present study will examine the effects of increasing dietary polyphenol intake by consumption of oregano and basil leaves, on plasma inflammatory and lipid factors and total urinary polyphenol levels in patients who have recently had unstable angina.

NCT07628348 — Effects of DRT on Neck Pain, ROM, and Chest Expansion in Patients With CR

StatusRecruiting
PhaseN/A
SponsorRiphah International University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsCervical Radiculopathy
Interventions;

This randomized controlled trial aims to determine the effects of the diaphragmatic release technique on neck pain, cervical range of motion, and chest expansion in patients with cervical radiculopathy. Participants will be randomized to either the baseline treatment or the experimental group for five weeks.

NCT07386418 — Study of Lesion-Specific Invasive Haemodynamic Angina Thresholds

StatusRecruiting
PhaseN/A
SponsorImperial College London
Enrollment60
Study TypeINTERVENTIONAL
ConditionsAngina (Stable); Coronary Artery Disease(CAD); Ischaemic Heart Disease (IHD)
Interventions;

ORBITA-SOLAR is an invasive physiological cardiac catheterisation study that aims to determine whether different coronary stenoses have different angina thresholds. The angina threshold is defined as the amount of coronary flow reduction required to reproduce symptoms. Sixty patients with symptoms of stable angina and 2 coronary artery stenoses amenable to percutaneous coronary intervention (PC…

NCT07626060 — Diagnostic Accuracy of GPT-4o and Claude for HEART Score Calculation in Chest Pain

StatusRecruiting
PhaseN/A
SponsorMarmara University Pendik Training and Research Hospital
Enrollment690
Study TypeOBSERVATIONAL
ConditionsEmergency Medicine; Artificial Intelligence (AI); Artificial Intelligence (AI) in Diagnosis; Chest Pain Rule Out Myocardial Infarction
Interventions; ;

This prospective observational diagnostic accuracy study evaluates whether large language models (LLMs) - GPT-4o (OpenAI, gpt-4o-2024-11-20) and Claude (Anthropic, claude-sonnet-4-6) - can accurately calculate HEART scores from unstructured Turkish clinical notes and predict 30-day major adverse cardiac events (MACE) in emergency department patients presenting with non-traumatic chest pain.

Th…

NCT07610408 — Comparison of IV Analgesia Protocols After the Regional Block’s Effect Diminishes in Thoracic Surgery

StatusRecruiting
PhaseN/A
SponsorAnkara Etlik City Hospital
Enrollment135
Study TypeINTERVENTIONAL
ConditionsPostoperative Pain After Thoracic Surgery; Postoperative Pain; Thoracic Surgery, Video Assisted; Patient Controlled Analgesia; Acute Pain
Interventions; ;

The purpose of this study is to compare the effectiveness of three different intravenous (IV) patient-controlled analgesia (PCA) regimens-Fentanyl, Tramadol, and Ibuprofen-in managing postoperative pain and respiratory performance in patients undergoing Video-Assisted Thoracoscopic Surgery (VATS). While regional blocks like Erector Spinae Plane (ESP) block provide effective early analgesia, the…

NCT07258290 — Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold (RMS) System in Subjects With Coronary Artery Lesions

StatusRecruiting
PhaseN/A
SponsorTeleflex
Enrollment1859
Study TypeINTERVENTIONAL
ConditionsCoronary Disease; Heart Diseases; Cardiovascular Diseases; Arteriosclerosis; Arterial Occlusive Diseases
Interventions;

The objective of this study is to assess the safety and efficacy of the Freesolve resorbable magnesium scaffold (RMS) in the treatment of subjects with up to two de novo lesions in native coronary arteries compared to the Xience coronary drug-eluting stent (DES) system

NCT07642336 — Erector Spinae Plane Block Versus Thoracic Epidural Analgesia for Open Liver Resection

StatusRecruiting
PhaseN/A
SponsorNguyen Toan Thang
Enrollment60
Study TypeINTERVENTIONAL
ConditionsLiver Neoplasms; Hepatic Resection; Liver Cancer
Interventions;

Background: Open liver resection is associated with severe postoperative pain. While thoracic epidural analgesia (TEA) is considered the gold standard for pain control, its clinical application is often limited by postoperative coagulation profile derangement, which increases the risk of epidural hematoma. Continuous erector spinae plane block (ESPB) has emerged as a promising, safer alternativ…

NCT07650877 — Comparison of the Rhomboid Intercostal Block and Serratus Posterior Superior Intercostal Plane Block

StatusRecruiting
PhaseN/A
SponsorAnkara City Hospital Bilkent
Enrollment90
Study TypeINTERVENTIONAL
ConditionsPain, Postoperative; Multimodal Analgesia; Rhomboid Intercostal Block; Serratus Posterior Superior Intercostal Plane Block; Thoracic Surgery, Video-Assisted
Interventions;

Video-assisted thoracic surgery (VATS) is widely performed for the management of various thoracic pathologies and is generally associated with reduced surgical trauma compared with open thoracotomy. Nevertheless, patients may still experience considerable postoperative pain, which can adversely affect respiratory function, mobilization, and recovery. Various regional analgesic techniques have b…

NCT07655336 — SPSIP Versus RISS Block in Volume-Preserving VATS

StatusRecruiting
PhaseN/A
SponsorFerit Yetik
Enrollment84
Study TypeINTERVENTIONAL
ConditionsPostoperative Pain; Thoracic Surgery
Interventions;

This prospective randomized controlled study aims to compare the effects of Serratus Posterior Superior Intercostal Plane (SPSIP) block and Rhomboid Intercostal and Subserratus (RISS) block on postoperative pain, respiratory function, and recovery quality in patients undergoing volume-preserving video-assisted thoracoscopic surgery (VATS). Eighty-four patients will be randomized in a 1:1 ratio …

NCT07235098 — Effect of a Music Intervention in Reducing Distress and Pain in Patients With Lung Cancer Undergoing Mini-invasive Surgery

StatusRecruiting
PhaseN/A
SponsorOncology Institute of Southern Switzerland
Enrollment74
Study TypeINTERVENTIONAL
ConditionsLung Cancer (Suspected or Confirmed)
Interventions

This study aims at evaluating whether music therapy intervention is effective in decreasing psychological (distress) and physical symptoms (pain) in patients with suspected or diagnosed lung cancer undergoing minimally invasive lung surgery.

NCT07632820 — Erector Spinae Plane Block Versus Trigger Point Injection for Chronic Thoracic Myofascial Pain

StatusRecruiting
PhasePhase 4
SponsorMayo Clinic
Enrollment76
Study TypeINTERVENTIONAL
ConditionsBack Pain
Interventions;

Chronic thoracic (mid-back) pain can be difficult to treat, and there is limited evidence to guide the use of injection therapies for pain arising from muscles and surrounding soft tissues. Two commonly used treatments are trigger point injections (TPI) and erector spinae plane (ESP) blocks, but no studies have directly compared their effectiveness for chronic thoracic myofascial pain. The purp…

Active, Not Recruiting

NCT03214510 — Thoracic Epidural Analgesia or Four-Quadrant Transversus Abdominus Plane Block in Reducing Pain in Patients Undergoing Liver Surgery

StatusActive, not recruiting
PhasePhase 3
SponsorM.D. Anderson Cancer Center
Enrollment101
Study TypeINTERVENTIONAL
ConditionsLiver and Intrahepatic Bile Duct Disorder
Interventions; ;

This phase III trial studies how well thoracic epidural analgesia or four-quadrant transversus abdominus plane block works in reducing pain in patients undergoing liver surgery. It is not yet known whether thoracic epidural analgesia or four-quadrant transversus abdominus plane block may help people to recover more completely and more quickly after surgery.

NCT06013722 — Strategy for Unstable Coronary Plaque in Patients Presenting to Emergency Department for Chest Pain Suspected of Coronary Artery Disease

StatusActive, not recruiting
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment22
Study TypeINTERVENTIONAL
ConditionsAtherosclerosis
Interventions

Primary prevention of coronary disease and especially its major complication, inaugural myocardial infarction, is based on any prodromal symptoms identification and on risk profile establishment. About 50% of myocardial infarctions are caused by an unstable non-stenosing plaque, asymptomatic before the event since without significant reduction in coronary flow, particularly during a stress test…

NCT05540223 — Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold System

StatusActive, not recruiting
PhaseN/A
SponsorBiotronik AG
Enrollment1861
Study TypeINTERVENTIONAL
ConditionsCoronary Artery Disease; Atherosclerosis, Coronary; Myocardial Ischemia; Ischemic Heart Disease; Acute Coronary Syndrome
Interventions;

The objective of this study is to assess the safety and efficacy of the Freesolve in the treatment of subjects with up to two de novo lesions in native coronary arteries compared to a contemporary drug eluting stent (DES).

NCT06701032 — Hemodynamic Parameters in People With Atherosclerotic Vascular Disease Referred to a Secondary Prevention and Cardiovascular Rehabilitation Program

StatusActive, not recruiting
PhaseN/A
SponsorLaval University
Enrollment80
Study TypeINTERVENTIONAL
ConditionsPeripheral Artery Disease (PAD); Coronary Artery Disease (CAD) (E.G., Angina, Myocardial Infarction, and Atherosclerotic Heart Disease (ASHD)); Cerebrovascular Atherosclerosis
Interventions

The main purpose of this study is to evaluate the hemodynamic changes in the forefoot of patients with coronary, cerebrovascular or peripheral atherosclerotic disease referred a 12-week cardiovascular rehabilitation program (PREV program).

Also, this study will describe the characteristics of patients admitted to the PREV program and their evolutions in terms of favorable, unfavorable outcomes…

NCT06853626 — One-hoUr Troponin Using a High-sensitivity Point-Of-Care Assay in Emergency Primary Care

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Oslo
Enrollment2500
Study TypeINTERVENTIONAL
ConditionsAcute Myocardial Infarction (AMI); Chest Pain; Acute Coronary Syndromes (ACS); Non-cardiac Chest Pain; Troponin
Interventions

Acute chest pain is a prevalent medical emergency in primary emergency care settings. Triage of chest pain prior to hospital admission presents significant challenges due to the absence of sufficiently sensitive diagnostic tools. Clinical signs, symptoms, risk assessment scores, or a normal electrocardiogram (ECG) can reliably exclude acute myocardial infarction (MI). This diagnostic uncertaint…

Not Yet Recruiting

NCT07668206 — Motivational Interviewing in Thoracic Outlet Syndrome

StatusNot yet recruiting
PhaseN/A
SponsorHacettepe University
Enrollment70
Study TypeINTERVENTIONAL
ConditionsThoracic Outlet Syndrome
Interventions;

The goal of this clinical trial is to learn if motivational interviewing (MI) works to improve symptoms in people with thoracic outlet syndrome (TOS). TOS is a condition that causes long-term pain, numbness, and weakness in the arm and shoulder area. The main questions it aims to answer are:

  • Does MI lower pain and improve arm function in people with TOS?
  • Does psychological resilience predi…

NCT07641400 — Pulmonary Artery Pressure in Predicting Pulmonary Embolism in Patients Presenting To The Emergency Department With Dyspnea

StatusNot yet recruiting
PhaseN/A
SponsorAntalya Health Sciences University
Enrollment80
Study TypeOBSERVATIONAL
ConditionsEmergency Department Patients; Pulmonary Hypertension; Pulmonary Embolism
Interventions;

The aim of this study is to determine the usability of echocardiographic PAP changes obtained from emergency department records in the early risk stratification of pulmonary embolism.

NCT07653932 — Perioperative Quantitative Sensory Testing and Incision Pain Mapping in Thoracic Surgery

StatusNot yet recruiting
PhaseN/A
SponsorTongji Hospital
Enrollment46
Study TypeOBSERVATIONAL
ConditionsPostoperative Pain; Chronic Postsurgical Pain; Thoracic Surgery; Lung Resection; Mechanical Hyperalgesia
Interventions

Postoperative pain remains a common and clinically important burden after thoracic surgery and may progress to chronic postsurgical pain. Conventional pain assessment mainly relies on patient-reported pain intensity and analgesic consumption, which may not fully capture peri-incisional sensory abnormalities, mechanical hyperalgesia, or central sensitization.

This prospective observational pilo…

NCT07643506 — Chest Tube-Delivered Bupivacaine to Decrease Postoperative Pain After Cardiac Surgery

StatusNot yet recruiting
PhaseEarly Phase 1
SponsorUniversity of Calgary
Enrollment60
Study TypeINTERVENTIONAL
ConditionsCoronary Artery Bypass Graft (CABG); Chest Tubes; Post Operative Pain Control
Interventions;

Background:

After heart surgery, patients require temporary chest tubes - plastic drains placed inside the chest to prevent fluid building up around the heart and lungs. These tubes are often very painful and can limit breathing, coughing, and movement, which necessitates usage of painkiller medication (opioids and non-steroidal anti-inflammatory drugs (NSAIDs)) that have negative side effects…

NCT07663435 — Influence of Superficial Parasternal Intercostal Plane Block on Internal Thoracic Artery Caliber to Facilitate Surgical Harvesting in CABG

StatusNot yet recruiting
PhasePhase 3
SponsorAin Shams University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsPain Management; Parasternal Block; CABG Graft Integrity
Interventions

Influence of Superficial Parasternal Intercostal Plane Block (SPIPB) on Internal Thoracic Artery (ITA) Caliber and Surgical Harvesting Efficiency in Coronary Artery Bypass Grafting (CABG)

NCT07684742 — Early Single Antiplatelet Therapy After IVUS-Guided PCI in Acute Coronary Syndrome

StatusNot yet recruiting
PhasePhase 4
SponsorGyeongsang National University Hospital
Enrollment1900
Study TypeINTERVENTIONAL
ConditionsAcute Coronary Syndromes; STEMI; NSTEMI; Unstable Angina
Interventions;

This is a prospective, open-label, multicenter, randomized, phase IV clinical trial designed to evaluate the safety and efficacy of early aspirin discontinuation followed by potent P2Y12 inhibitor monotherapy after intravascular ultrasound (IVUS)-guided drug-eluting stent implantation in patients with acute coronary syndrome. A total of 1,900 patients who achieve complete revascularization afte…

NCT07687082 — Prevalence and Risk Factors for Chronic Post-Surgical Pain Following Video-Assisted Thoracic Surgery : The EVATHO Prospective Bicentric Cohort Study.

StatusNot yet recruiting
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment400
Study TypeOBSERVATIONAL
ConditionsChronic Post-surgical Pain; Postoperative Pain After Thoracic Surgery; Neuropathic Pain; Thoracic Surgical Procedures

Chronic post-surgical pain (CPSP) remains a common complication after thoracic surgery and may significantly impair patients’ quality of life. Although the widespread adoption of video-assisted thoracic surgery (VATS) has reduced surgical trauma and improved postoperative recovery, a substantial proportion of patients still develop persistent pain.

The EVATHO study is a multicenter prospective…

NCT07653204 — Contactless Ultrasound Data Acquisition in Emergency Departments to Discriminate the Origin of Dyspnea and Chest Pain

StatusNot yet recruiting
PhaseN/A
SponsorAustral Diagnostics
Enrollment2500
Study TypeOBSERVATIONAL
ConditionsDyspnea; Chest Pain
Interventions

PAnDA-One is a prospective, multicenter, interventional study (10 centers, France) aimed at developing and validating a diagnostic support algorithm based on the ADx-One medical device, which non-invasively acquires thoracic vibrations using airborne ultrasound.

The study will enroll 2,500 patients presenting to the emergency department with acute dyspnea or non-traumatic chest pain, divided i…

Enrolling by Invitation

NCT07658521 — Combined SPSP and TTP Blocks for Postoperative Analgesia Post-CABG

StatusEnrolling by invitation
PhaseN/A
SponsorAin Shams University
Enrollment88
Study TypeINTERVENTIONAL
ConditionsPostoperative Pain Following Coronary Artery Bypass Grafting (CABG)
Interventions; ;

The goal of this clinical trial is to learn if combining two ultrasound-guided nerve blocks - one for the front of the chest and one for the side of the chest - works better than standard pain medications alone to treat pain after coronary artery bypass grafting (CABG) surgery. It will also learn about the safety of these nerve blocks. The main questions it aims to answer are:

Does the combine…

Completed Trials

NCT00982176 — Determinants of Cognitive Impairment After Acute Coronary Syndrome

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Bordeaux
Enrollment49
Study TypeINTERVENTIONAL
ConditionsCoronary Syndrome
Interventions

The general purpose of the present pathophysiological study is to investigate the relation between cognitive impairment observed after an acute coronary syndrome and the presence of cerebral anatomo-functional abnormalities. This study will improve the investigators’ understanding of the disease and will help in early diagnosis and prevention of vascular dementia in this population.

NCT01293019 — Osteopathic Treatment in Adult Patients With Cystic Fibrosis

StatusCompleted
PhasePhase 3
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment32
Study TypeINTERVENTIONAL
ConditionsCystic Fibrosis; Back Pain; Neck Pain; Chest Pain
Interventions; ;

To study the contribution of osteopathy on the reduction of pain in adult patients with cystic fibrosis

NCT04580017 — Prognostic Accuracy of the HEART Score in Undifferentiated Chest Pain: A Multicenter Validation Study

StatusCompleted
PhaseN/A
SponsorUniversity of Monastir
Enrollment4267
Study TypeOBSERVATIONAL
ConditionsCoronary Disease; Coronary Syndrome; Risk Factor, Cardiovascular; Major Adverse Cardiovascular Events

Chest pain remains one of the most common, potentially serious presenting complaints for adults emergency department visits with approximately 7.6 million yearly visits in the united states. The priority for emergency physician is to determine whether these patients with acute chest pain have a potential life threatening underlying etiology. The great challenge is to differentiate patients pres…

NCT04465669 — Heterogeneity of Neointimal Healing Following Biodegradable-polymer Drug-Eluting Coronary Stent Implantation

StatusCompleted
PhaseN/A
SponsorTomsk National Research Medical Center of the Russian Academy of Sciences
Enrollment50
Study TypeINTERVENTIONAL
ConditionsCoronary Heart Disease; Stable Angina Pectoris; Silent Myocardial Ischemia
Interventions;

The objective of this study is a comparative evaluation of Orsiro stent and of Resolute Integrity stent in terms of the extent of neointima formation at 4 months after implantation using optical coherence tomography (OCT).

NCT07647822 — Comparison of Early Postoperative Functional Capacity and Kinesiophobia in Patients Undergoing Thoracic Surgery Via Thoracotomy or VATS

StatusCompleted
PhaseN/A
SponsorHacettepe University
Enrollment18
Study TypeOBSERVATIONAL
ConditionsVATS; Kinesiophobia; Thoracotomy; Thoracic Surgery

This observational cross-sectional study aims to compare early postoperative functional capacity and kinesiophobia in patients undergoing thoracic surgery via thoracotomy or video-assisted thoracic surgery (VATS). Patients aged 18-75 years who underwent thoracic surgery and agreed to participate will be evaluated during the early postoperative period, after chest tube removal and before hospita…

NCT07634731 — Bilateral RSB vs TEA Epidural Analgesia for Postoperative Pain Control After Open Gastrectomy: A Randomized Controlled Trial

StatusCompleted
PhaseN/A
SponsorIgors Ivanovs
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBilateral Rectus Sheath Block; Thoracic Epidural Analgesia
Interventions

Patients indicated for elective open gastrectomy were screened, enrolled, and randomised between October 2021 and September 2023. The patients were randomised to either Group A (intervention-continuous bupivacaine) or Group B (control-NaCl saline). The primary outcome measures were the quantity of an opioid analgesic administered during the initial 72 h post-surgery and the level of postoperati…

NCT07532564 — Risk Factors, Costs, and Impacts of ED Boarding

StatusCompleted
PhaseN/A
SponsorUniversity of Maryland, Baltimore
Enrollment30486
Study TypeOBSERVATIONAL
ConditionsStroke (CVA) or TIA; Diabetes; Asthma (Diagnosis); COPD (Chronic Obstructive Pulmonary Disease); Sepsis

The goal of this observational study is to learn about the risk factors, costs, and operational impacts of emergency department boarding (patients admitted to the hospital but remaining in the emergency department awaiting placement on an inpatient floor)

The main questions it aims to answer is:

  1. What characteristics of patients make them more likely to experience ED boarding?
  2. What is th…

NCT06035731 — Evaluation of the Medical Service by Socio-aesthetics in Oncology

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier de Valence
Enrollment400
Study TypeINTERVENTIONAL
ConditionsCancer of Colon; Cancer, Lung; Cancer, Breast; Cancer Prostate; Cancer Pain
Interventions

the 3-year randomized controlled RCT-SE study aims to investigate Socio-aesthetics well being care on quality of life, pain and anxiety.

The primary objective is to show that socio-aesthetics well being care improves quality of life during cancer treatment, compared to self care administration of dermo-cosmetics products

The secondary objectives are to show that socio-aesthetics well being ca…

NCT07653230 — Two Bupivacaine Concentrations for Erector Spinae Plane Block in Percutaneous Nephrolithotomy

StatusCompleted
PhaseN/A
SponsorAnkara Education and Research Hospital
Enrollment60
Study TypeOBSERVATIONAL
ConditionsPercutaneous Nephrolithotomy (PNL); Nephrolithiasis
Interventions

People who undergo percutaneous nephrolithotomy (PNL), a procedure used to remove kidney stones, often experience pain after surgery. An ultrasound-guided erector spinae plane block (ESPB) is commonly used to help reduce this pain.

This study compares two different concentrations of bupivacaine, a local anesthetic medication, used during ESPB. Participants undergoing PNL will receive either 0….

NCT07287761 — Comparison of Erector Spinae Plane Block and Serratus Posterior Superior Intercostal Plane Block in Postoperative Pain Management After Coronary Artery Bypass Grafting

StatusCompleted
PhaseN/A
SponsorAnkara Education and Research Hospital
Enrollment55
Study TypeOBSERVATIONAL
ConditionsPostoperative Pain After Thoracic Surgery; Coronary Artery Bypass Graft (CABG)

Coronary Artery Bypass Grafting (CABG) is a common surgical procedure for ischemic heart disease, but it often leads to severe acute and chronic postoperative pain, which can delay recovery and reduce patient comfort. Effective pain management is crucial to prevent pulmonary complications and long hospital stays. Peripheral nerve blocks are increasingly used to reduce opioid consumption and imp…

NCT07098962 — KinesioTaping for Thoracic Drain Support

StatusCompleted
PhasePhase 2 / Phase 3
SponsorKastamonu University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsPrimary Condition: Pain, Postoperative; Associated Conditions: Cardiac Surgical Procedures, Thoracic Surgery
Interventions;

This study investigates the effectiveness of KinesioTaping applied around mediastinal and thoracic drain sites in reducing postoperative pain after cardiac surgery. Effective pain management is critical for early mobilization, improved patient satisfaction, and prevention of respiratory complications such as atelectasis. KinesioTaping is theorized to support soft tissue healing, improve circula…

NCT07671196 — Validity and Reliability of Arabic Version of Extended Aberdeen Spine Pain Scale

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment300
Study TypeOBSERVATIONAL
ConditionsNonspecific Spinal Pain (Including Cervical, Thoracic, and Lumbar Spinal Pain)

The goal of this observational study is to determine whether the Arabic version of the Extended Aberdeen Spine Pain Scale (EASPS) is a valid and reliable tool for assessing spine-related pain and functional disability in Arabic-speaking adults with nonspecific spinal pain.

The main questions it aims to answer are:

  • Is the Arabic version of the EASPS a valid instrument for evaluating spine-re…

Other (Terminated)

NCT02829736 — ThOracoscopic Wedge Resection Treated With Chest Tube Removal Intraoperatively

StatusTerminated
PhaseN/A
SponsorRigshospitalet, Denmark
Enrollment25
Study TypeINTERVENTIONAL
ConditionsPain; Decreased Lung Function; Delayed Discharge
Interventions; ;

Chest tubes are used routinely although preliminary studies demonstrate the feasibility and safety of intraoperative chest drain removal. Previous studies are however either retrospective or mainly concerning benign disease.

Hypothesis: Participants treated without post-operative chest tube after thoracoscopic wedge resection have less pain, better pulmonary function and similar complication p…