Viewing Study NCT01292759


Ignite Creation Date: 2025-12-24 @ 3:01 PM
Ignite Modification Date: 2025-12-25 @ 3:33 PM
Study NCT ID: NCT01292759
Status: UNKNOWN
Last Update Posted: 2011-02-15
First Post: 2011-02-09
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Non-invasive Assessment of Arterial Blood Pressure and Functional Hemodynamic Parameters
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'CASE_ONLY'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 24}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2010-07'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2010-07', 'lastUpdateSubmitDate': '2011-02-14', 'studyFirstSubmitDate': '2011-02-09', 'studyFirstSubmitQcDate': '2011-02-09', 'lastUpdatePostDateStruct': {'date': '2011-02-15', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2011-02-10', 'type': 'ESTIMATED'}}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['stroke volume', 'cardiac output', 'validation'], 'conditions': ['Surgical Procedure, Unspecified']}, 'descriptionModule': {'briefSummary': 'Cardiac output can be monitored using different invasive devices. Nexfin HD is a new, noninvasive device that uses model flow technology to measure stroke volume and thus computes cardiac output (CO). To evaluate this new device the investigators compared esophageal doppler CO to Nexfin HD CO in patients scheduled for elective abdominal surgery.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '80 Years', 'minimumAge': '18 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Patients scheduled for elective abdominal surgery', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Age \\> 18 and \\< 80 years old\n* Written informed consent obtained\n\nExclusion Criteria:\n\n* Renal failure\n* Heart failure (EF \\< 25%)\n* Peripheral artery occlusion disease\n* M. Raynaud\n* Rhythms other than sinus'}, 'identificationModule': {'nctId': 'NCT01292759', 'briefTitle': 'Non-invasive Assessment of Arterial Blood Pressure and Functional Hemodynamic Parameters', 'organization': {'class': 'OTHER', 'fullName': 'Johannes Gutenberg University Mainz'}, 'officialTitle': 'An Evaluation of a New, Non-invasive Monitoring Device in Major Abdominal Surgery Patients', 'orgStudyIdInfo': {'id': '837.194.10 (7203)'}}, 'contactsLocationsModule': {'locations': [{'zip': '55131', 'city': 'Mainz', 'status': 'RECRUITING', 'country': 'Germany', 'contacts': [{'name': 'Larissa Philippi', 'role': 'CONTACT', 'email': 'l.philippi@web.de'}], 'facility': 'Klinik für Anaesthesiology der Universitätsmedizin Mainz', 'geoPoint': {'lat': 49.98185, 'lon': 8.28008}}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Johannes Gutenberg University Mainz', 'class': 'OTHER'}, 'responsibleParty': {'oldNameTitle': 'Larissa Philippi', 'oldOrganization': 'Klinik für Anästhesie'}}}}