Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'DIAGNOSTIC', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 40}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2022-03-01', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2022-08', 'completionDateStruct': {'date': '2022-06-15', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2022-08-01', 'studyFirstSubmitDate': '2022-07-25', 'studyFirstSubmitQcDate': '2022-07-26', 'lastUpdatePostDateStruct': {'date': '2022-08-03', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2022-07-27', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2022-05-31', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Peripherial venous pressure as an indicator of central venous pressure', 'timeFrame': '3 months'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Peripherial venous pressure', 'Central venous pressure'], 'conditions': ['Peripherial Venous Pressure', 'Central Venous Pressure', 'Fluid/Volume Status Monitoring of Patient']}, 'descriptionModule': {'briefSummary': 'The study is aimed at comparing peripherial venous pressure as an indicator of central venous pressure in post operative surgical patients.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '75 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* ASA I/II/III surgical patients who require central venous access as part of their surgical treatment plan with no organ support in post operative period.\n* Age between 18 and 75 years\n* Who have atleast 1 x 18 gauge peripherial venous cannula in the upper limb from elbow below to the hand\n* Who have given consent\n\nExclusion Criteria:\n\n* Not meeting the inclusion criteria'}, 'identificationModule': {'nctId': 'NCT05476666', 'briefTitle': 'Peripheral Venous Pressure as an Indicator of Central Venous Pressure in Post Operative Surgical Patients: A Randomised Controlled Trial', 'organization': {'class': 'OTHER', 'fullName': 'Pakistan Navy Station Shifa Hospital'}, 'officialTitle': 'Peripheral Venous Pressure as an Indicator of Central Venous Pressure in Post Operative Surgical Patients: A Randomised Controlled Trial', 'orgStudyIdInfo': {'id': 'ERC/2022/ANS/1'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Pressures measured', 'description': 'Venous pressure measured through a peripherial and a central venous catheter/cannula', 'interventionNames': ['Procedure: Peripherial and central venous access']}], 'interventions': [{'name': 'Peripherial and central venous access', 'type': 'PROCEDURE', 'description': 'Passing a peripherial and a central venous catheter/cannula', 'armGroupLabels': ['Pressures measured']}]}, 'contactsLocationsModule': {'locations': [{'zip': '46000', 'city': 'Karachi', 'state': 'Sindh', 'country': 'Pakistan', 'facility': 'PNS Shifa Hospital', 'geoPoint': {'lat': 24.8608, 'lon': 67.0104}}], 'overallOfficials': [{'name': 'Kenan Khan', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Pakistan Navy Station Shifa Hospital'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Pakistan Navy Station Shifa Hospital', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Graded Anaesthetist, Principal Investigator', 'investigatorFullName': 'Kenan Anwar Khan', 'investigatorAffiliation': 'Pakistan Navy Station Shifa Hospital'}}}}