[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"non-erosive-gastro-esophageal-reflux-disease\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:non-erosive-gastro-esophageal-reflux-disease":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":42,"leadSponsor":44,"locationsCount":5},"100645553","quality-of-sleep-improvement-with-evening-topical-therapy-for-non-erosive-gastroesophageal-reflux-disease-the-quiet-trial-100645553",false,"NCT07700342","QUality of Sleep Improvement With Evening Topical Therapy for Non-Erosive Gastroesophageal Reflux Disease (The QUIET Trial)","QUality of Sleep Improvement With Evening Topical Therapy for Non-Erosive Gastroesophageal Reflux Disease: Results of a Single-center, Randomized, Double-blind, Placebo-controlled Study (The QUIET Trial)","QUIET","Inclusion Criteria:\n\n1. Diagnosis of gastroesophageal reflux disease based on the presence of typical symptoms of heartburn and\u002For regurgitation at least 6 months before the screening visit, confirmed by the investigator.\n2. Erosive reflux disease (ERD), Barrett's esophagus, and other esophageal abnormalities confirmed by gastroscopy within the last 6 months by the investigator based on medical records.\n3. Use of proton pump inhibitors in a single morning dose for at least two months prior to study entry, with an inadequate response to these medications for nocturnal symptoms of gastrointestinal reflux, and with at least moderate sleep quality disturbances, as defined by the PSQI (Pittsburgh Sleep Quality Index) score of 5-10 points - moderate sleep disturbances. 4. Not using the following medications within the month prior to the screening visit: H2 blockers, prokinetics (itopride, prucalopride), GLP1\u002FGIP analogues, antibiotics, baclofen, tricyclic antidepressants, serotonin and\u002For norepinephrine reuptake inhibitors, and\u002For the following medications within the week prior to the screening visit: sucralfate, antacids, and esophageal protective agents. 5. Severity of gastroesophageal reflux symptoms that reduce the patient's quality of life, as subjectively confirmed by the patient. 6. Age ≥18 years of life at the time of the screening visit. 7. At the screening visit, women of childbearing potential must not be pregnant (confirmed by a urine pregnancy test) and must not be breastfeeding, or must be of non-reproductive potential (surgically sterilized, physiologically incapable of conceiving, or at least one year postmenopausal, i.e., amenorrheic for 12 consecutive months). 8. Women of childbearing potential who have a male partner of fertile potential must use a highly effective method of contraception from the screening visit until 18 weeks after the last dose of the investigational drug. 9. Men who have sex with women of childbearing potential must agree to use barrier contraceptive methods (condoms) or abstain from sexual intercourse throughout the study, beginning at the screening visit and for at least 7 days after the last dose of the investigational medical device. 10. Ability to participate in all aspects of this clinical trial. 11. A male or female patient who is able to voluntarily give informed consent.\n\n   \\-\n\n   Exclusion Criteria:\n\n1\\. Women who have started lactation or have a positive urine test confirming pregnancy during the study enrollment visit.2. Introduction of significant changes in diet and lifestyle during the study.3. Presence of warning signs during the study enrollment visit: dysphagia or odynophagia, unintentional weight loss of more than 5% of initial weight, symptoms of gastrointestinal bleeding, anemia, upper abdominal tumor, and persistent vomiting for 7-10 days.4. Planned use during the study: antibiotics, pro-\u002Fpre-\u002Fsynbiotics, short-chain fatty acids, proton pump inhibitors, H2 blockers, prokinetics (itopride, prucalopride), GLP1\u002FGIP analogues, antibiotics, baclofen, tricyclic antidepressants, serotonin and\u002For norepinephrine reuptake inhibitors, and one week before the start of the study: sucralfate, antacids, and preparations protecting the esophageal mucosa.5. Diagnosis of a serious illness (e.g., cancer). 6. : Planned hospitalization for any reason or diagnosis of any serious concomitant disease which, in the opinion of the investigator, is a contraindication to participation in the study or may compromise the safety of the patient. Translated with DeepL.com (free version) 7. Current or recent (within one year prior to randomization) history of alcohol dependence or psychoactive substance abuse.8. Active psychiatric problems that, in the investigator's opinion, may interfere with compliance with study procedures.9. Presence of unstable or uncontrolled cardiovascular disorders, moderate or severe heart failure (NYHA class III or IV), any pulmonary, hepatic, renal, gastrointestinal, genitourinary, hematopoietic, coagulation, immunological, endocrine\u002Fmetabolic disorders, or other medical disorders that, in the opinion of the investigator, could affect the results of the study or compromise the safety of the patient.10. Any person who:a. Is an employee of the study site, investigator, study organization, or Sponsor.b. Is a first-degree relative of an employee of the study site, investigator, CRO, or Sponsor.c. Is unable to attend all study visits or comply with study procedures.Translated with DeepL.com (free version)\n\n\\-","ALL","18 Years",{"count":20,"type":21},50,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this randomized, double-blind, single-center clinical trial is to learn if medical devices work to decrease nocturnal symptoms of GERD gastroesophageal reflux disease in adults' patients and improve sleeping time, quality of sleep and quality of life of patients with nocturnal GERD symptoms. It will also teach us about safety, tolerability and improvement of patient's quality of life during and after taking medical device. The main questions it aims to answer are:\n\n* Does medical device relieve reflux symptoms during night sleep?\n* Does medical device improve the quality of sleep and quality of life life of patients with GERD symptoms? Researchers will compare medical device to a placebo (a look-alike substance that contains no drug) to see if medical device works in nocturnal GERD gastroesophageal reflux disease.\n\nParticipants will:\n\n* Take medical device or a placebo every day just before sleeping (1 times a day) for 14 days\n* Visit the clinic 2 times during 14 days of this study for checkups and tests\n* Keep a diary of their symptoms and the number of times they use a medical device\n* Fill out the form to collect all necessary data. Medical device or placebo will be prepared in same looking sachets of 10 ml liquid. Medical device or placebo will be administered orally, at a dose of 10 ml one time daily just before bedtime for 14 days. The liquid should be drunk slowly, in small sips direct from the sachets.",[27,28,29,30],"Nocturnal Symptoms of GERD","Sleep Disorders in GERD","GERD (Gastroesophageal Reflux Disease)","Non-Erosive Gastro-Esophageal Reflux Disease",[32,33,34,35],"Sleep disturbances in reflux disease","Sleep disorders in GERD","Quality of sleep in GERD","NERD","RECRUITING","2026-07-09",{"date":39,"type":40},"2026-07-14","ACTUAL",{"date":37,"type":21},{"date":43,"type":21},"2026-09-30",{"name":45,"class":46},"Cellmedis","INDUSTRY",{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":64,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":80},"100382135","real-life-study-of-changes-of-gastroesophageal-reflux-disease-manifestations-due-to-behavioural-and-diet-adherence-100382135","NCT04255693","Real-life Study of Changes of Gastroesophageal Reflux Disease Manifestations Due to Behavioural and Diet Adherence","Inclusion Criteria:\n\n* willingness to participate (based on the signed informed consent form);\n* presence of gastroesophageal reflux disease, based on the following: a) typical symptoms, like heartburn and\u002For regurgitation (for primary selection, symptoms should be present at least weekly, be actual for at least 3 months prior to the enrolment, and the patient should report the history of symptoms which lasts for at least 6 months); b) previous response to the intake of proton pump inhibitors; c) data of 24-hours oesophageal pH-impedance monitoring with detected pathological gastroesophageal reflux according to the Lyon consensus definitions;\n\nExclusion Criteria:\n\n* pregnant or breast-feeding females;\n* abdominal or chest surgery (except appendectomy or cholecystectomy in case they are not followed by adhesive disease of the abdominal organs);\n* constant use of non-steroidal anti-inflammatory agents (NSAIDs), sporadic use of NSAIDs will be allowed in case the course of treatment was discontinued at least 2 weeks prior to the enrolment, in case that constant use of NSAIDs happen to be necessary after the enrolment, the patients may continue in the study but doses, frequency and duration of treatment should be carefully documented;\n* history or current evidence of cancer of any aetiology and location besides skin cancer in situ successfully treated before the enrolment;\n* severe patient's conditions which may lead to misinterpretation of data, or in case of patient's enrolment may put him at risk of exacerbation of co-morbid conditions, or in cases when on discretion of the investigator patient's condition would not allow him to complete the course of the observation. These conditions include, but not limited to: heart failure (class III-IV by NYHA), uncontrolled hypertension, severe neurological disorders, decompensated liver cirrhosis (Child-Pugh B or C), severe depression or other psychological disorders;\n* the patient may stop his participation in the study at any time by informing the site personal about his\u002Fher decision to withdraw the consent.","80 Years",{"count":55,"type":21},150,[24],"This study is aimed to investigate the role of long-term diet adherence on manifestations of gastroesophageal reflux disease",[59,60,61,62,63,30],"Gastroesophageal Reflux Disease","GERD","Gastroesophageal Erosion","Erosive Esophagitis","Non-erosive Reflux Disease",[60,35,65,66,67,68,69],"erosive esophagitis","diet","food","adherence","influence","2025-08-01",{"date":72,"type":40},"2025-08-03",{"date":74,"type":40},"2020-01-31",{"date":76,"type":21},"2027-12-31",{"name":78,"class":79},"Federal State Budgetary Scientific Institution \"Federal Research Centre of Nutrition, Biotechnology","OTHER",1]