{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Digestive+Well+Being&page=21", "query": { "condition": "Digestive Well Being", "page": 21 }, "page_size": 10 }, "pagination": { "page": 21, "page_size": 10, "total_count": 552, "total_pages": 56, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Digestive+Well+Being&page=22&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Digestive+Well+Being&page=20&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-21T23:34:40.590Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT05685758", "title": "A Treatment for Depression Via a Gamified Mobile Phone Application Based on a New Cognitive Model", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression", "Depressive Disorder", "Clinical Depression", "Major Depressive Disorder" ], "interventions": [ { "name": "FTP-based therapeutic mobile-app", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Hedonia Ltd", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "20 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "20 Years to 50 Years" }, "enrollment_count": 117, "start_date": "2022-11-03", "completion_date": "2023-07-31", "has_results": false, "last_update_posted_date": "2023-10-13", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05685758" }, { "nct_id": "NCT02043184", "title": "Improving Adherence to Oral Cancer Agents and Self Care of Symptoms Using an IVR", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prostatic Neoplasms", "Breast Neoplasms", "Colorectal Neoplasms", "Melanoma", "Leukemia" ], "interventions": [ { "name": "Interactive Voice Response (IVR) Reminders", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Michigan State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 322, "start_date": "2013-03", "completion_date": "2016-07", "has_results": false, "last_update_posted_date": "2017-06-07", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 8, "location_summary": "New Haven, Connecticut • Chicago, Illinois • Indianapolis, Indiana + 4 more", "locations": [ { "city": "New Haven", "state": "Connecticut" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Ann Arbor", "state": "Michigan" }, { "city": "Lansing", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT02043184" }, { "nct_id": "NCT03028584", "title": "Survivorship Care Plans in a Community Oncology Practice", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Cancer", "Prostate Cancer", "Colorectal Cancer" ], "interventions": [ { "name": "Survey", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Wisconsin, Madison", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 30, "start_date": "2017-09-11", "completion_date": "2018-03-23", "has_results": false, "last_update_posted_date": "2019-11-18", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 1, "location_summary": "Waukesha, Wisconsin", "locations": [ { "city": "Waukesha", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT03028584" }, { "nct_id": "NCT00739752", "title": "Interventions to Increase HBV Vaccinations in Sexually Transmitted Disease (STD) Clinics", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hepatitis B Virus" ], "interventions": [ { "name": "Non-Framed-Offered", "type": "BEHAVIORAL" }, { "name": "Non-Framed-Recommended", "type": "BEHAVIORAL" }, { "name": "Gain-Framed-Offered", "type": "BEHAVIORAL" }, { "name": "Gain-Framed-Recommended", "type": "BEHAVIORAL" }, { "name": "Loss-Framed-Offered", "type": "BEHAVIORAL" }, { "name": "Loss-Framed-Recommended", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1747, "start_date": "2003-06", "completion_date": "2007-10", "has_results": true, "last_update_posted_date": "2018-11-09", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 2, "location_summary": "Chicago, Illinois • Indianapolis, Indiana", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT00739752" }, { "nct_id": "NCT03313414", "title": "HCV Post-Exposure Prophylaxis for Health Care Workers", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Hepatitis C" ], "interventions": [ { "name": "Sofosbuvir/Velpatasvir Treatment for 14 days", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2019-08-13", "completion_date": "2020-01-16", "has_results": false, "last_update_posted_date": "2020-01-21", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03313414" }, { "nct_id": "NCT06582849", "title": "Enhanced Assistance During Radiotherapy for Unmet Essential Needs", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bone Cancer", "Brain Cancer", "Colorectal Cancer", "Esophagus Cancer", "Lymphoma", "Salivary Gland Cancer", "Head and Neck Cancer", "Liver Cancer", "Ovarian Cancer", "Pancreatic Cancer", "Prostate Cancer", "Small Intestine Cancer", "Stomach Cancer", "Urinary Bladder Cancer", "Anal Cancer", "Blood Cancer", "Breast Cancer", "Cervical Cancer", "Lung Cancer", "Kidney Cancer", "Penile Cancer", "Skin Cancer", "Testicular Cancer", "Thyroid Cancer", "Uterine Cancer", "Vaginal Cancer", "Vulvar Cancer" ], "interventions": [ { "name": "Standard assistance", "type": "OTHER" }, { "name": "Enhanced assistance", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 33, "start_date": "2024-10-04", "completion_date": "2025-08-08", "has_results": false, "last_update_posted_date": "2025-08-26", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT06582849" }, { "nct_id": "NCT07516587", "title": "Study to Investigate the Efficacy of a Digestive Health Dietary Supplement on Post-meal Bloating in Healthy Participants", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Digestive Health", "Abdominal Discomfort", "Gas and Bloating" ], "interventions": [ { "name": "Bloat Gummies", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebo", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "Arrae", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 100, "start_date": "2026-04", "completion_date": "2026-10", "has_results": false, "last_update_posted_date": "2026-04-13", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07516587" }, { "nct_id": "NCT05115916", "title": "Effect of Patient Portal Messaging Before Mailing Fecal Immunochemical Testing Kit on Colorectal Cancer Screening Rates", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colorectal Cancer", "Colorectal Neoplasms", "Colorectal Cancer Screening" ], "interventions": [ { "name": "MyChart Priming Message", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "51 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "51 Years to 75 Years" }, "enrollment_count": 3880, "start_date": "2019-08-28", "completion_date": "2020-12-20", "has_results": false, "last_update_posted_date": "2021-11-10", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 1, "location_summary": "Westwood, Los Angeles, California", "locations": [ { "city": "Westwood, Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05115916" }, { "nct_id": "NCT02949947", "title": "Efficacy of Ferric Carboxymaltose in Gastrointestinal Stromal Tumor (GIST) Patients With Iron Deficiency Anemia (IDA) Receiving Systemic Therapy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Malignant Neoplasms of Mesothelial and Soft Tissue", "Gastrointestinal Stromal Tumor With Neurogenic Differentiation" ], "interventions": [ { "name": "Ferric Carboxymaltose", "type": "DRUG" }, { "name": "Iron Supplements", "type": "DIETARY_SUPPLEMENT" }, { "name": "Questionnaire", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "DIETARY_SUPPLEMENT", "BEHAVIORAL" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3, "start_date": "2017-12-18", "completion_date": "2019-03-06", "has_results": true, "last_update_posted_date": "2020-04-06", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02949947" }, { "nct_id": "NCT01203462", "title": "The PRIDE Study Probiotics on Regulation and Improving Digestive hEalth", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Digestive Irregularity", "Digestive Discomfort", "History of Straining During Bowel Movements", "History of Hard or Lumpy Stools" ], "interventions": [ { "name": "Probiotic strain of Bifidobacterium", "type": "OTHER" }, { "name": "No Bifidobacterium", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Georgetown University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 68, "start_date": "2010-10", "completion_date": "2011-07", "has_results": false, "last_update_posted_date": "2013-02-11", "last_synced_at": "2026-10-21T23:34:40.590Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01203462" } ] }