Ignite Creation Date:
2025-12-25 @ 2:51 AM
Ignite Modification Date:
2026-02-28 @ 11:20 PM
Study NCT ID:
NCT03680833
Status:
UNKNOWN
Last Update Posted:
2018-09-26
First Post:
2018-09-14
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Sentinel Node Detection in Cervical Cancer
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2018-09-14', 'size': 705891, 'label': 'Study Protocol and Statistical Analysis Plan', 'hasIcf': False, 'hasSap': True, 'filename': 'Prot_SAP_000.pdf', 'typeAbbrev': 'Prot_SAP', 'uploadDate': '2018-09-20T09:33', 'hasProtocol': True}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'DIAGNOSTIC', 'interventionModel': 'SINGLE_GROUP', 'interventionModelDescription': 'prospective cohort study'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 226}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2014-06-15', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2018-09', 'completionDateStruct': {'date': '2021-12', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2018-09-24', 'studyFirstSubmitDate': '2018-09-14', 'studyFirstSubmitQcDate': '2018-09-20', 'lastUpdatePostDateStruct': {'date': '2018-09-26', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2018-09-21', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2020-12', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Sentinel node detection in cervical cancer; Sensitivity and negative predictive values for identifying pelvic nodal disease, See detailed study protocol', 'timeFrame': '4-5 years', 'description': 'Detection of Sentinel nodes followed by full pelvic lymphadenectomy'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Sentinel Lymph Node Biopsy']}, 'descriptionModule': {'briefSummary': 'Evaluation of sensitivity of Sentinel lymph nodes for detecting nodal metastases in cervical cancer', 'detailedDescription': 'Consecutive women with stage 1a2-2a1 cervical cancer scheduled for surgery will be approached for eligibility by defined criteria.\n\nSentinel nodes will be detected by a combined use of Indocyanine green and Tc99 radiocolloid ( first 75 patients) and for the continuation with either the combined use or the best performing of those tracers.\n\nTechnical success rates, adverse events (related study intervention and overall) sensitivity and negative predictive values will be estimated.\n\nAn interim analyse will be performed after 34 node positive patients based on the Fleming two stage analyse. The null hypothesis of sensitivity of 85% will be tested against an estimated sensitivity of 95%. At this stage the study may be closed for futility, closed as hull hypothesis is rejected or continued to reach another 28 node positive patients.\n\nAs a full pelvic lymphadenectomy will be performed after detection of sentinel nodes patient will act ast their own controls.'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '80 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Women of age 18 years and older at the time of informed consent.\n* Women with a pathologically proven cervical carcinoma of any histologic subtype, clinically stage 1a2- 2a1 planned for primary surgery\n* Absence of any exclusion criteria\n\nExclusion Criteria:\n\n* Non consenting patients\n* Ongoing pregnancy\n* Inability to understand written and/or oral study information\n* Who performance status III or more\n* Previous lower limb lymphedema\n* Surgical contraindication to a laparoscopic approach or lymphadenectomy at surgeons discretion.\n* Anesthesiologic contraindication to a laparoscopic approach at the anesthetist's discretion\n* Locally advanced disease or intraabdominal/distant metastases at preoperative CT, MRI or ultrasonography\n* Radiologically suspect pelvic nodal metastatic disease according to the RECIST criteria (\\>= 1 node with \\>=16 mm short axis diameter)\n* Allergy to Iodine\n* Patients with a known liver disease\n* Patients with a significant bleeding disorder or mandatory antithrombotic treatment."}, 'identificationModule': {'nctId': 'NCT03680833', 'acronym': 'SLNcxca', 'briefTitle': 'Sentinel Node Detection in Cervical Cancer', 'organization': {'class': 'OTHER', 'fullName': 'Region Skane'}, 'officialTitle': 'Sentinel Node Detection in Cervical Cancer', 'orgStudyIdInfo': {'id': 'RegionSkaneKKLund2'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'OTHER', 'label': 'prospective cohort study', 'description': 'Prospective cohort study with detection of sentinel lymph nodes followed by a full pelvic lymphadenectomy. Patients will act as their own controls.\n\nThe intervention is the detection and removal of sentinel lymph nodes', 'interventionNames': ['Procedure: Sentinel node detection in cervical cancer']}], 'interventions': [{'name': 'Sentinel node detection in cervical cancer', 'type': 'PROCEDURE', 'description': 'The study intervention is the injection of tracer followed by detection and removal of sentinel lymph nodes', 'armGroupLabels': ['prospective cohort study']}]}, 'contactsLocationsModule': {'locations': [{'zip': '22185', 'city': 'Lund', 'status': 'RECRUITING', 'country': 'Sweden', 'contacts': [{'name': 'Jan Persson, ass professor', 'role': 'CONTACT', 'email': 'jan.persson@med.lu.se', 'phone': '+46733522080'}, {'name': 'Linnea Ekdahl, MD', 'role': 'CONTACT', 'email': 'linnea.ekdahl@med.lu.se', 'phone': '+46739292631'}], 'facility': 'Department of Gynecology and Obstetrics', 'geoPoint': {'lat': 55.70584, 'lon': 13.19321}}], 'centralContacts': [{'name': 'Jan Persson, ass professor', 'role': 'CONTACT', 'email': 'jan.persson@med.lu.se', 'phone': '+46733522080'}, {'name': 'Linnea Ekdahl, MD', 'role': 'CONTACT', 'email': 'linnea.ekdahl@med.lu.se', 'phone': '0739292631'}], 'overallOfficials': [{'name': 'Jan Persson, ass professor', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Region Skane'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Region Skane', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR'}}}}