Viewing Study NCT06879912


Ignite Creation Date: 2025-12-26 @ 11:08 AM
Ignite Modification Date: 2025-12-31 @ 8:54 PM
Study NCT ID: NCT06879912
Status: RECRUITING
Last Update Posted: 2025-10-16
First Post: 2025-03-11
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: A Study to Understand the Utility of the Force Feedback Instruments in Robotic Procedures Using da Vinci 5 Robot
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006552', 'term': 'Hernia, Inguinal'}, {'id': 'D006555', 'term': 'Hernia, Ventral'}], 'ancestors': [{'id': 'D046449', 'term': 'Hernia, Abdominal'}, {'id': 'D006547', 'term': 'Hernia'}, {'id': 'D020763', 'term': 'Pathological Conditions, Anatomical'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'OTHER'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 200}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2025-05-22', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-10', 'completionDateStruct': {'date': '2026-08', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-10-14', 'studyFirstSubmitDate': '2025-03-11', 'studyFirstSubmitQcDate': '2025-03-11', 'lastUpdatePostDateStruct': {'date': '2025-10-16', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2025-03-17', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2026-08', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'To assess the force imparted on the tissue by force feedback instruments.', 'timeFrame': 'Intra-operative'}], 'secondaryOutcomes': [{'measure': 'To evaluate the utility of force feedback instruments during specific procedural steps or tasks.', 'timeFrame': 'Post-operative prior to discharge'}]}, 'oversightModule': {'isUsExport': False, 'oversightHasDmc': False, 'isFdaRegulatedDrug': False}, 'conditionsModule': {'conditions': ['Hernia, Inguinal', 'Hernia, Ventral', 'Colorectal', 'Thoracic', 'Gynecologic', 'Partial Nephrectomy']}, 'descriptionModule': {'briefSummary': 'The goal of this observational study is to understand the utility of force feedback instruments in surgeries that are done using the da Vinci 5 robot.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '22 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Subjects who will undergo the study specified procedure as primary procedure with da Vinci 5 robot and who meet all eligibility criteria will be considered for enrollment.', 'healthyVolunteers': False, 'eligibilityCriteria': 'Pre-Operative Inclusion Criteria:\n\n1. Age 22 years or older\n2. ASA ≤ 3\n3. The clinical decision has been made to perform multi-port robotic assisted surgery with da Vinci 5 with Force Feedback instruments for the study specified procedure as primary procedure prior to enrollment in the study\n4. Subject or a legally authorized representative is able to provide written informed consent using the study informed consent form prior to the study\n5. Subject is willing and able to comply with the study protocol requirements including follow up schedule\n\nPre-operative Exclusion Criteria:\n\n* Subject receiving an emergent procedure\n* Subject planned to undergo major concomitant surgery for the treatment of a different medical condition than was originally planned\n* Subject with previous ipsilateral surgery (open, endoscopic or robotic) with the same surgical indication\n* Subject with past or ongoing medical conditions (for example: inflammatory bowel disease) which, in the judgment of the Investigator, puts them at high risk for surgery and not appropriate for the study\n* Subject is pregnant or suspected to be pregnant or breastfeeding\n* Subject has any other condition or personal circumstance that, in the judgment of the Investigator, might interfere with the collection of complete quality data\n* Subject is currently participating in or has participated in a study of an investigational agent or a significant risk investigational device study within the past 6 months\n* Subject belongs to a vulnerable population.\n* Subject is contraindicated for anesthesia or surgery.\n* Subject has had previous neoadjuvant therapy, previous chemotherapy, immunotherapy, and/or radiation therapy for the treatment of the cancer to be resected within the past 6 months\n\nIntra-operative Exclusion Criteria\n\n* Subject with hemodynamic or respiratory instability, which precludes the Investigator from performing the RAS.\n* Subject in whom inadequate visualization makes a minimally invasive approach not feasible, as determined from the investigator assessment prior to docking the robot.\n* Subject with adhesions, scarring and disease status in the body which in the opinion of the investigator limits the ability to perform the minimally invasive procedure.'}, 'identificationModule': {'nctId': 'NCT06879912', 'briefTitle': 'A Study to Understand the Utility of the Force Feedback Instruments in Robotic Procedures Using da Vinci 5 Robot', 'organization': {'class': 'INDUSTRY', 'fullName': 'Intuitive Surgical'}, 'officialTitle': 'A Prospective, Post-Market Study to Evaluate the Clinical Utility of the Force Feedback Instruments in RAS Procedures Using the da Vinci 5 Surgical System', 'orgStudyIdInfo': {'id': 'ISI-dV5-MP-01'}}, 'contactsLocationsModule': {'locations': [{'zip': '43210', 'city': 'Columbus', 'state': 'Ohio', 'status': 'RECRUITING', 'country': 'United States', 'contacts': [{'name': 'Clinical Research Manager', 'role': 'CONTACT', 'email': 'kayla.diaz@osumc.edu', 'phone': '614-293-8549'}, {'name': 'Robert Merritt', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Ohio State University', 'geoPoint': {'lat': 39.96118, 'lon': -82.99879}}, {'zip': '78758', 'city': 'Austin', 'state': 'Texas', 'status': 'RECRUITING', 'country': 'United States', 'contacts': [{'name': 'Division Research Manager', 'role': 'CONTACT', 'email': 'Krishna.Saini@stdavids.com', 'phone': '512.544.8070'}, {'name': 'Thiru Lakshman', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': "St. David's Healthcare", 'geoPoint': {'lat': 30.26715, 'lon': -97.74306}}], 'centralContacts': [{'name': 'Smruthi Srinivasa Murthy', 'role': 'CONTACT', 'email': 'smruthi.srinivasamurthy@intusurg.com', 'phone': '682-552-6131'}, {'name': 'Manish Bharara', 'role': 'CONTACT', 'email': 'manish.bharara@intusurg.com'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Intuitive Surgical', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}