[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"war-related-injuries\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:war-related-injuries":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,51],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":32,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100571143","confirming-the-effects-of-acupuncture-treatments-to-relieve-symptoms-of-gulf-war-illness-100571143",false,"NCT06716411","Confirming the Effects of Acupuncture Treatments to Relieve Symptoms of Gulf War Illness","CARE","Inclusion Criteria:\n\n* Deployed to the Gulf Theater of operations (as defined by 38 CFR 3.317, includes Iraq, Kuwait, Saudi Arabia, Bahrain, Qatar, the United Arab Emirates, Oman, the Gulf of Aden, the Gulf of Oman, the Persian Gulf, the Arabian Sea, the Red Sea, and the airspace above all of these locations) between August 1990 and the present date\n* Have at least 2 of the following symptoms from the 3 CDC clusters of symptom that have lasted for more than 6 months. Each symptom cluster must be characterized as mild-moderate or severe, with at least one symptom in each cluster required to be severe. The clusters are:\n\nA. Fatigability: fatigue 24 hours or more after exertion B. Mood and Cognition: feeling depressed; feeling irritable; difficulty thinking or concentrating; feeling worried, tense, anxious; problems finding words; or problems getting to sleep C. Musculoskeletal: joint pain or muscle pain\n\nExclusion Criteria:\n\n* Currently enrolled in another clinical trial\n* Have another disease that likely could account for the symptoms, as determined by our Medical Monitor\n* Severe psychiatric illness (in the last 2 years psychiatric hospitalization, suicidal attempt, alcohol or substance abuse, use of antipsychotic medication) as measured by the Primary Care Evaluation of Mental Disorder (Prime MD).\n* Unable to complete the protocol on based on the evaluation of the Medical Monitor.","ALL","18 Years",{"count":19,"type":20},200,"ESTIMATED","INTERVENTIONAL",[23],"NA","This unblinded Phase II clinical trial will test the effects of individualized acupuncture treatments offered in extant acupuncture practices in the community; practitioners will have had at least 5 years of experience plus additional training provided by the study. Veterans with diagnosed symptoms of Gulf War Illness will be randomized to either six months of biweekly acupuncture treatments (group 1, n=100) or 2 months of waitlist followed by weekly acupuncture treatments (group 2, n=100). Measurements were taken at baseline, 2, 4 and 6 months. The primary outcome is the SF-36 physical component scale score (SF-36P).",[26,27,28,29,30,31],"Persian Gulf Syndrome","Gulf War Syndrome","Multiple Chronic Illnesses","Occupational Diseases","War-Related Injuries","Wounds and Injuries",[33,34,35,36,37],"Acupuncture","Gulf War Illness","Complex Medical Illness","Chronic Multisymptom Illness","Veteran","RECRUITING","2026-04-02",{"date":41,"type":42},"2026-04-03","ACTUAL",{"date":44,"type":42},"2026-02-03",{"date":46,"type":20},"2028-09-30",{"name":48,"class":49},"University of Utah","OTHER",10,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":59,"enrollmentInfo":60,"targetDuration":62,"studyType":63,"phases":4,"briefSummary":64,"conditions":65,"keywords":68,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":83},"100629425","from-battlefield-to-recovery-continuous-regional-anaesthesia-for-war-related-lower-limb-trauma-100629425","NCT07474506","From Battlefield to Recovery: Continuous Regional Anaesthesia for War-Related Lower Limb Trauma","From Battlefield to Recovery: Continuous Regional Anaesthesia for War-Related Lower Limb Trauma - A Multicenter Comparative Cohort Study","CRA-WAR-LIMB S","Inclusion Criteria:\n\n* age ≥18 years\n* war-related lower limb trauma\n* hospital admission requiring surgical treatment or wound management\n* documented pain assessment during hospitalization\n* availability of analgesic treatment data\n* informed consent where required\n\nExclusion Criteria:\n\n* age \\\u003C18 years\n* isolated upper limb trauma\n* missing key pain outcome data\n* contraindication to regional anaesthesia prior to treatment\n* refusal to participate (for prospective component)","50 Years",{"count":61,"type":20},150,"6 Weeks","OBSERVATIONAL","To compare the effectiveness of continuous regional anaesthesia with standard pain management strategies for the treatment of acute pain in patients with war-related lower limb trauma.",[66,67,30],"Pain Management","Perioperative Analgesia",[69,70,71,72],"acute pain","pain managment","analgesia","war related trauma","NOT_YET_RECRUITING","2026-03-14",{"date":76,"type":42},"2026-03-17",{"date":78,"type":20},"2026-03-15",{"date":80,"type":20},"2026-06-15",{"name":82,"class":49},"Charitable Organisation Charitable Fund Superhumans (Co Cf Superhumans)",1]