[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pectus-excavatum\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pectus-excavatum":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,54,79,108,130,163,187,208,233,256],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100054298","spsipb-versus-sapb-for-postoperative-analgesia-after-minimally-invasive-repair-of-pectus-excavatum-100054298",false,"NCT07697222","SPSIPB Versus SAPB for Postoperative Analgesia After Minimally Invasive Repair of Pectus Excavatum","Comparison of the Postoperative Analgesic Effects of Serratus Posterior Superior Intercostal Plane Block and Serratus Anterior Plane Block After Minimally Invasive Repair of Pectus Excavatum: A Prospective Observational Cohort Study","Inclusion Criteria:\n\n* Patients aged 15 to 25 years\n* Diagnosis of pectus excavatum\n* Scheduled to undergo minimally invasive repair of pectus excavatum under general anesthesia\n* Receipt of either bilateral serratus posterior superior intercostal plane block or bilateral serratus anterior plane block as part of routine perioperative analgesic care\n* Written informed consent obtained from the patient or, for patients younger than 18 years, from a legal guardian\n\nExclusion Criteria:\n\n* Refusal to participate in the study\n* Contraindication to regional anesthesia\n* Known allergy to local anesthetics or study analgesic medications\n* Chronic opioid use\n* Pre-existing chronic pain syndrome\n* Coagulopathy or use of anticoagulant therapy that contraindicates regional block application\n* Local infection at the block injection site\n* Neurological or psychiatric condition that may interfere with pain assessment\n* Incomplete perioperative or postoperative data\n* Conversion to another surgical technique or major intraoperative complication requiring a change in the routine analgesic protocol","ALL","15 Years","25 Years",{"count":20,"type":21},80,"ESTIMATED","7 Days","OBSERVATIONAL","This prospective observational cohort study will compare postoperative analgesic outcomes in patients undergoing minimally invasive repair of pectus excavatum. Participants will be grouped according to the regional analgesia technique applied as part of routine clinical care: serratus posterior superior intercostal plane block or serratus anterior plane block. The primary outcome will be total opioid consumption during the first 24 hours after surgery. Secondary outcomes will include postoperative pain scores, rescue analgesic requirement, opioid-related adverse effects, patient satisfaction, mobilization time, and length of hospital stay.",[26,27],"Pectus Excavatum","Chest Deformities",[29,30,31,32,33,34,35,36,37,38,39,40],"Pectus excavatum","Serratus Anterior Plane Block","Serratus Posterior Superior Intercostal Plane Block","Opioid-Free Anesthesia","Multimodal Analgesia","SAP Block","SPSIP Block","Postoperative Pain","Opioid-Related Adverse Effects","Opioid Consumption","Chest Deformity Surgery","Regional Anesthesia","RECRUITING","2026-07-06",{"date":44,"type":45},"2026-07-13","ACTUAL",{"date":47,"type":45},"2026-06-22",{"date":49,"type":21},"2027-06",{"name":51,"class":52},"Marmara University","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":16,"minAge":61,"maxAge":4,"enrollmentInfo":62,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":64,"conditions":65,"keywords":68,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":53},"100615282","phrenic-infiltration-as-cryoanalgesia-adjuvant-for-early-postoperative-pain-following-the-nuss-procedure-100615282","NCT07290582","Phrenic Infiltration as Cryoanalgesia Adjuvant for Early Postoperative Pain Following the Nuss Procedure","PHABULA","Inclusion Criteria:\n\n* patients who undergo minimally invasive repair at the pediatric surgery department of our referral tertiary center\n\nExclusion Criteria:\n\n* patients who refuse OR whose parents refuse to participate in the study","14 Years",{"count":63,"type":21},50,"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:\n\nDoes the addition of phrenic Infiltration as Cryo Adjuvant (PhICA) to earlier percutaneous intercostal cryoanalgesia (EPIC) reduce postoperative pain scores compared to EPIC alone? Does the combined EPIC + PhICA technique reduce the need for rescue tramadol compared to EPIC alone? Do the two approaches differ in: length of hospital stay, time to transition to oral therapy, and time to mobilization? Are there any side effects\n\nResearchers will compare patients who received EPIC alone to patients who received EPIC + PhICA to see if the combined technique provides superior pain control.\n\nParticipants:\n\nReceived either EPIC alone or EPIC combined with PhICA as part of their surgical anesthesia plan Had pain levels assessed using the Numeric Rating Scale (NRS) at regular postoperative intervals Were monitored for rescue tramadol requirements, medicaments taken, length of hospital stay, and mobilization timing Were monitored for any technique-related complication",[26,66,67],"Cryo Analgesia","Phrenic Nerve-related Diaphragmatic Impairment",[69],"cryoanalgesia pectus phrenic","2026-06-13",{"date":72,"type":45},"2026-06-16",{"date":74,"type":45},"2023-09-14",{"date":76,"type":21},"2026-08-15",{"name":78,"class":52},"Papa Giovanni XXIII Hospital",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":16,"minAge":61,"maxAge":87,"enrollmentInfo":88,"targetDuration":90,"studyType":23,"phases":4,"briefSummary":91,"conditions":92,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":53},"100640924","the-bridge-pain-study-100640924","NCT07602595","The BRIDGE Pain Study","Biopsychosocial Risk Influences on the Development and Generation of Early-Onset Chronic Pain","BRIDGE","Inclusion Criteria:\n\n* Diagnosis of rheumatic\u002Fautoimmune disease\u002Fpain condition or surgery prior to age 18; Current age 14 to 26 years; Participant (and parent\u002Flegal guardian of participants \\\u003C 18 yo) can read and write in English; At least 1 year from diagnosis of pain or rheumatic disease; For individuals with MSK surgical history, at least 1 year after initial surgical intervention; For individuals with rheumatic disease, their disease must be considered inactive\n\nExclusion Criteria:\n\n* They have active disease, or Other major medical comorbidities have developed after surgery following MSK surgical intervention.","26 Years",{"count":89,"type":21},600,"4 Weeks","The purpose of the study is to discover at least two distinct Musculoskeletal pain subtypes. These types are caused by different brain-and-immune system signals that affect how the body feels pain, and they are also shaped by a person's biology, psychology, and social environment.\n\nAim 1. We want to sort adolescents and young adults with long lasting muscle and bone pain into two different groups. To do this, we will look at participants' childhood medical histories, past treatments, when their pain started, the sex they were assigned at birth, what their pain feels like now, tests of how their body senses pain, and immune system markers found in their blood. We think we will find at least two different types of chronic pain groups, plus one group of patients who had a higher risk for pain (because of a rheumatic disease or past surgery) but never developed long term pain.\n\nAim 2. We want to find out if certain patterns of inflammation in the body change how nerve cells react to pain.\n\nAim 3: We want to understand how different biological, psychological, and social factors are connected to the chronic pain groups we identified. We think we will find certain mental, behavioral, and social risks-as well as protective factors-that help explain why some people develop long-lasting pain and others do not. We expect these factors to play different roles in each pain group, including the group that does not develop chronic pain.",[93,94,95,96,26,97,98],"Juvenile Idiopathic Arthritis (JIA)","Fibromyalgia","Lupus","Scoliosis","Chronic Pain","Musculoskeletal Pain","2026-05-16",{"date":101,"type":45},"2026-05-22",{"date":103,"type":21},"2026-08",{"date":105,"type":21},"2029-08",{"name":107,"class":52},"Children's Hospital Medical Center, Cincinnati",{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":16,"minAge":115,"maxAge":116,"enrollmentInfo":117,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":119,"conditions":120,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":53},"100586670","field-test-and-psychometric-validation-of-the-pectus-excavatum-evaluation-questionnaire-in-the-dutch-pectus-excavatum-population-100586670","NCT06918392","Field-test and Psychometric Validation of the Pectus Excavatum Evaluation Questionnaire in the Dutch Pectus Excavatum Population","TRANSLATE","Inclusion Criteria:\n\n* Eligible participants will be pectus excavatum patients aged 12 to 18 years old who are scheduled for a Nuss procedure. Parents or legal guardians will also be invited to complete the parent section of the PEEQ.\n\nExclusion Criteria:\n\n* Exclusion criteria will be the inability of the patient or their parent\u002Fguardian to complete the corresponding section of the questionnaire due to language barriers.","12 Years","18 Years",{"count":118,"type":21},66,"A questionnaire that can measure disease severity from the patients perspective in patients with pectus excavatum already exists in English (Pectus Excavatum Evaluation Questionnaire; PEEQ). This questionnaire was recently translated into Dutch. Before this Dutch version can be used, it needs to be tested by a number of patients.\n\nData will be collected at three moments:\n\n1. Preoperatively: The PEEQ will be completed on paper during the outpatient clinic visit.\n2. Postoperatively: The PEEQ will be completed electronically 2 months post-surgery.\n3. Test-retest reliability: The PEEQ will be administered electronically at least two weeks after a previous assessment.",[26],"2026-03-23",{"date":123,"type":45},"2026-03-25",{"date":125,"type":45},"2021-12-15",{"date":127,"type":21},"2026-11-30",{"name":129,"class":52},"Erik de Loos",{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":135,"acronym":136,"eligibilityCriteria":137,"healthyVolunteers":11,"sex":16,"minAge":138,"maxAge":4,"enrollmentInfo":139,"targetDuration":4,"studyType":141,"phases":142,"briefSummary":144,"conditions":145,"keywords":148,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":53},"100626130","intraoperative-cryoanalgesia-versus-thoracic-epidural-block-in-mirpe-minimally-invasive-repair-of-pectus-excavatum-100626130","NCT07431632","Intraoperative Cryoanalgesia Versus Thoracic Epidural Block in MIRPE (Minimally Invasive Repair of Pectus Excavatum)","Comparative Study of the Efficacy of Intraoperative Intercostal Cryoanalgesia and Thoracic Epidural Block in the Postoperative Period of Minimally Invasive Pectus Excavatum Repair (MIRPE): a Prospective, Randomized Clinical Trial","FROZEN MIRPE","Inclusion Criteria:\n\n1. Having pectus excavatum;\n2. Having signed the Informed Consent Form for the study.\n\nExclusion Criteria:\n\n1. Age \\\u003C 13 years at the time of the procedure;\n2. Chronic use of analgesics preoperatively;\n3. Pectus carinatum, Poland syndrome, or other chest wall anomalies;\n4. Previous pectus excavatum repair by any technique;\n5. Previous thoracic surgery;\n6. Congenital heart disease;\n7. Hemorrhagic dyscrasia;\n8. Major anesthetic risk factors or history of previous problems with anesthesia;\n9. Pregnancy.","13 Years",{"count":140,"type":21},40,"INTERVENTIONAL",[143],"NA","The main objective of this study is to compare epidural blockade with cryoanalgesia of the intercostal nerves as an analgesic method in the postoperative period of minimally invasive repair of pectus excavatum (MIRPE).",[146,26,147,36],"Funnel Chest","Postoperative Pain After Video Assisted Thoracic Surgery",[149,150,151,152,153],"cryoanalgesia","pectus excavatum","funnel chest","postoperative pain","MIRPE","2026-02-18",{"date":156,"type":45},"2026-02-24",{"date":158,"type":45},"2024-11-28",{"date":160,"type":21},"2028-01",{"name":162,"class":52},"University of Sao Paulo",{"id":164,"slug":165,"hasResults":11,"nctId":166,"briefTitle":167,"officialTitle":168,"acronym":169,"eligibilityCriteria":170,"healthyVolunteers":11,"sex":16,"minAge":171,"maxAge":116,"enrollmentInfo":172,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":173,"conditions":174,"keywords":175,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":178,"lastUpdatePostDateStruct":179,"startDateStruct":181,"completionDateStruct":183,"leadSponsor":185,"locationsCount":53},"100616963","comparative-analysis-of-modified-vs-classical-nuss-technique-in-the-surgical-correction-of-pectus-excavatum--100616963","NCT07312448","Comparative Analysis Of Modified Vs. Classical Nuss Technique In The Surgical Correction Of Pectus Excavatum \"","Single-Center Retrospective Comparative Analysis Of Modified Vs. Classical Nuss Technique In The Surgical Correction Of Pectus Excavatum \"","PE","Inclusion Criteria:\n\n* Patients aged 11 to 18 years.\n* Patients who underwent surgery between 2010 and 2024 using either the classic or modified Nuss technique. - Patient with a Haller index of 2.25 or higher.\n\nExclusion Criteria:\n\n* Patients with a Haller score below 2.25.\n* Patients who have undergone surgery using alternative techniques such as Ravitch or modified Ravitch.\n* Patients under 11 years of age or over 19 years of age.","11 Years",{"count":20,"type":21},"Although the NUSS technique has become the standard minimally invasive procedure for correcting this deformity, there is a lack of comparative data between the classic and modified NUSS techniques. This research aims to fill this gap by comparing these two methods in terms of various outcomes, such as operative time, postoperative pain control, length of stay in the intensive care unit, and overall cosmetic results.\n\nThis study addresses the need to optimize surgical techniques to improve patient outcomes. By evaluating these two approaches, the research seeks to provide insights that could lead to better management strategies for patients with pectus excavatum, potentially influencing future clinical practices.",[26],[26,176,177],"Nuss techniques","Modified Nuss Technique","2025-12-30",{"date":180,"type":45},"2025-12-31",{"date":182,"type":45},"2024-12-02",{"date":184,"type":21},"2026-02",{"name":186,"class":52},"University Hospital, Strasbourg, France",{"id":188,"slug":189,"hasResults":11,"nctId":190,"briefTitle":191,"officialTitle":192,"acronym":4,"eligibilityCriteria":193,"healthyVolunteers":11,"sex":16,"minAge":115,"maxAge":194,"enrollmentInfo":195,"targetDuration":4,"studyType":141,"phases":197,"briefSummary":198,"conditions":199,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":200,"lastUpdatePostDateStruct":201,"startDateStruct":203,"completionDateStruct":205,"leadSponsor":207,"locationsCount":53},"100568513","es-catheter-vs-cryoablation-after-pectus-surgery-100568513","NCT06682208","ES Catheter vs Cryoablation After Pectus Surgery","Prospective Randomized Trial of Efficacy and Safety of Erector Spinae Catheter and Intercostal Nerve Cryoablation Protocols After Pectus Surgery","Inclusion Criteria:\n\n* Age 12 - 21 years\n* History of pectus excavatum\n* Scheduled for Nuss procedure\n\nExclusion Criteria:\n\n* Prior pectus repair\n* Other concomitant surgeries\n* Chronic pain conditions including Ehlers Danlos Syndrome\n* Non-English speaking - rationale: the questionnaires used in the study are in English language and the social and cultural factors of pain perception of non-English speaking patients could affect the study power\n* Severe developmental delays including cognitive (difficulties understanding), motor (cerebral palsy or muscular dystrophy), and speech delays (difficulties communicating)\n* History of or active renal or liver disease\n* Major surgery requiring opioids in the last 2 years\n* Severe respiratory problems (such as obstructive sleep apnea, cystic fibrosis, pulmonary fibrosis, or pneumonia within the last month)\n* Cardiac conditions including, but not limited to, cyanotic heart disease, hypoplastic left ventricle, arrhythmia, uncontrolled hypertension with ongoing treatment, Kawasaki disease, or cardiomyopathies. Participants with asymptomatic valvular lesions or defects may be included\n* BMI \\>35\n* Pregnant or breastfeeding females","21 Years",{"count":196,"type":21},176,[143],"Participants will be randomized to receive ES catheter or cryoablation for pain management after the Nuss procedure. The goal of this study is to compare the following between the two groups:\n\n* Time to achieve short-term physical therapy goals and long-term functional outcomes\n* Compare immediate and long-term postoperative opioid use\n* Compare numbness on chest of postoperative day 1 and the return of sensation to baseline\n* Compare the incidence of neuropathic pain and other complications\n\nParticipants will receive surveys for up to 12 months postoperatively.",[26],"2025-09-17",{"date":202,"type":45},"2025-09-18",{"date":204,"type":45},"2024-04-08",{"date":206,"type":21},"2029-04",{"name":107,"class":52},{"id":209,"slug":210,"hasResults":11,"nctId":211,"briefTitle":212,"officialTitle":213,"acronym":4,"eligibilityCriteria":214,"healthyVolunteers":215,"sex":16,"minAge":115,"maxAge":216,"enrollmentInfo":217,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":219,"conditions":220,"keywords":222,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":225,"lastUpdatePostDateStruct":226,"startDateStruct":228,"completionDateStruct":230,"leadSponsor":232,"locationsCount":53},"100599217","percutaneous-intercostal-cryoneuromodulation-onset-timing-100599217","NCT07081620","Percutaneous Intercostal Cryoneuromodulation Onset Timing.","How Long Does it Take for Percutaneous Intercostal Cryoneuromodulation to Produce Cryoanalgesia? A Prospective Observational Study.","Inclusion Criteria:\n\n* Patients who are undergoing preoperative percutaneous intercostal cryoneurolysis for pectus excavatum surgery\n\nExclusion Criteria:\n\n* failure to obtain consent",true,"40 Years",{"count":218,"type":21},20,"Percutaneous Intercostal Cryoneurolysis is a promising technique that addresses acute postoperative pain after Nuss procedure for pectus excavatum. However its onset timing has not yet been determined. A physical examination would assess the variation of chest skin sensitivity to soft touch, cold (water at 4°C), and heat (water at 40°C) through days following the cryoneurolysis procedure.",[221,26],"Cryotherapy Effect",[223,224],"Cryoneurolysis","Cryoneuromodulation","2025-07-22",{"date":227,"type":45},"2025-07-23",{"date":229,"type":45},"2025-06-07",{"date":231,"type":21},"2026-11",{"name":78,"class":52},{"id":234,"slug":235,"hasResults":11,"nctId":236,"briefTitle":237,"officialTitle":238,"acronym":239,"eligibilityCriteria":240,"healthyVolunteers":11,"sex":16,"minAge":115,"maxAge":116,"enrollmentInfo":241,"targetDuration":4,"studyType":141,"phases":242,"briefSummary":243,"conditions":244,"keywords":245,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":247,"lastUpdatePostDateStruct":248,"startDateStruct":250,"completionDateStruct":252,"leadSponsor":254,"locationsCount":53},"100588008","effectiveness-of-one-minute-versus-two-minute-cryoanalgesia-in-nuss-surgery-100588008","NCT06935799","Effectiveness of One-Minute Versus Two-Minute Cryoanalgesia in Nuss Surgery","Effectiveness of One-Minute Versus Two-Minute Cryoanalgesia in Nuss Surgery: A Pilot Randomized Controlled Trial","Cryo-One","Inclusion Criteria:\n\n* Pectus excavatum repair with MIRPE\n* Written consent for corrective surgery with intraoperative cryoanalgesia\n* Written consent to participate in the study\n* Age \\>12 and \\\u003C 18 years\n\nExclusion Criteria:\n\n* History of previous thoracic surgeries\n* Reoperation for chest deformity\n* Contraindication for cryoanalgesia\n* Presence of other conditions that may affect the course of the procedures and the assessment of their effectiveness and safety",{"count":140,"type":21},[143],"Intercostal nerve cryoanalgesia has become a popular method for managing postoperative pain after Nuss procedure, showing greater effectiveness compared to epidural anesthesia and patient-controlled analgesia. However, the optimal duration of cryoanalgesia remains unknown. Most protocols use a two-minute cryoablation, although histological studies show similar changes with both one-minute and two-minute applications.\n\nThis is a pilot, single-center, randomized, double-blind study comparing the effectiveness of one-minute versus two-minute cryoanalgesia in treating pain in patients undergoing correction of pectus excavatum using the Nuss procedure. The aim of the project is to evaluate the validity of the research procedure and determine the sample size for the main study. Preliminary data on postoperative pain intensity, opioid consumption, duration of surgery, length of hospital stay, and complications will be analyzed.",[26,146],[149,246,150,151],"pain management","2025-04-28",{"date":249,"type":45},"2025-05-01",{"date":251,"type":45},"2025-04-25",{"date":253,"type":21},"2026-03",{"name":255,"class":52},"Children's Memorial Health Institute, Poland",{"id":257,"slug":258,"hasResults":11,"nctId":259,"briefTitle":260,"officialTitle":261,"acronym":4,"eligibilityCriteria":262,"healthyVolunteers":11,"sex":263,"minAge":264,"maxAge":61,"enrollmentInfo":265,"targetDuration":4,"studyType":141,"phases":267,"briefSummary":268,"conditions":269,"keywords":270,"overallStatus":277,"whyStopped":4,"lastUpdateSubmitDate":278,"lastUpdatePostDateStruct":279,"startDateStruct":281,"completionDateStruct":282,"leadSponsor":284,"locationsCount":53},"100564892","investigation-of-the-effectiveness-of-telerehabilitation-training-in-pectus-excavatum-deformity-100564892","NCT06635083","Investigation of the Effectiveness of Telerehabilitation Training in Pectus Excavatum Deformity","Comparison of the Effects of Vacuum Bell Therapy and Additional Telerehabilitation on Physical Fitness, Respiratory Functions, Posture and Psychosocial Factors in Children with Pectus Excavatum : a Single-Blind Randomized Controlled Trial","Inclusion Criteria:\n\n* Children aged 10-14\n* Boys\n* Those who have undergone Vacuum Bell treatment for the first time\n\nExclusion Criteria:\n\n* Those with complex type pectus deformity\n* Those who have undergone any surgical treatment due to pectus excavatum\n* Those with chronic systemic disease (cardiovascular, gastrointestinal, metabolic)\n* Those with diagnosed serious psychiatric disease\n* Those with scoliosis over 20 degrees\n* Those with other musculoskeletal anomalies and connective tissue disorders (Marfan syndrome, Turner syndrome, neurofibromatosis tuberous sclerosis)\n* Those with neurological disease\n* Those with hearing or vision impairment that cannot be corrected with hearing aids or glasses\n* Those who do not have internet access or do not own a tablet\u002Fcomputer","MALE","10 Years",{"count":266,"type":21},62,[143],"The aim of this study is to investigate the effectiveness of telerehabilitation-based exercise training in addition to Vacuum Bell therapy on physical fitness, respiratory functions, posture and psychosocial factors in boys aged between 10-14 years diagnosed with pectus excavatum.",[26],[271,272,273,274,275,276],"Telerehabilitation","Posture","Congenital Abnormalities","Quality of Life","Physical Fitness","Respiratory Function Tests","NOT_YET_RECRUITING","2024-10-08",{"date":280,"type":45},"2024-10-10",{"date":280,"type":21},{"date":283,"type":21},"2025-04-30",{"name":285,"class":52},"Eastern Mediterranean University"]