Viewing Study NCT02271360


Ignite Creation Date: 2025-12-25 @ 2:02 AM
Ignite Modification Date: 2026-04-19 @ 9:04 AM
Study NCT ID: NCT02271360
Status: COMPLETED
Last Update Posted: 2017-02-16
First Post: 2014-10-19
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Calcium Dobesilate Versus Cabergoline for Prevention of Ovarian Hyperstimulation Syndrome
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D007246', 'term': 'Infertility'}], 'ancestors': [{'id': 'D000091662', 'term': 'Genital Diseases'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D002123', 'term': 'Calcium Dobesilate'}, {'id': 'D000077465', 'term': 'Cabergoline'}], 'ancestors': [{'id': 'D001557', 'term': 'Benzenesulfonates'}, {'id': 'D001555', 'term': 'Benzene Derivatives'}, {'id': 'D006841', 'term': 'Hydrocarbons, Aromatic'}, {'id': 'D006844', 'term': 'Hydrocarbons, Cyclic'}, {'id': 'D006838', 'term': 'Hydrocarbons'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D001190', 'term': 'Arylsulfonates'}, {'id': 'D017739', 'term': 'Arylsulfonic Acids'}, {'id': 'D013451', 'term': 'Sulfonic Acids'}, {'id': 'D013456', 'term': 'Sulfur Acids'}, {'id': 'D013457', 'term': 'Sulfur Compounds'}, {'id': 'D004873', 'term': 'Ergolines'}, {'id': 'D004876', 'term': 'Ergot Alkaloids'}, {'id': 'D000470', 'term': 'Alkaloids'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}, {'id': 'D006576', 'term': 'Heterocyclic Compounds, 4 or More Rings'}, {'id': 'D000072471', 'term': 'Heterocyclic Compounds, Fused-Ring'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2', 'PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['PARTICIPANT']}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 200}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2014-04', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2017-02', 'completionDateStruct': {'date': '2015-12', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2017-02-14', 'studyFirstSubmitDate': '2014-10-19', 'studyFirstSubmitQcDate': '2014-10-21', 'lastUpdatePostDateStruct': {'date': '2017-02-16', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2014-10-22', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2015-12', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Number of participants with ovarian hyperstimulation syndrome (OHSS)', 'timeFrame': 'weekly for eight weeks', 'description': 'this will be assessed by:\n\nClinically:\n\nAbdominal bloating Mild abdominal pain Nausea ± vomiting Oliguria Acute respiratory distress syndrome\n\nBy ultrasound Ovarian size usually ˃8 cm Ultrasound evidence of ascites\n\nLaboratory Haemoconcentration haematocrit ˃45% Hypoproteinaemia'}], 'secondaryOutcomes': [{'measure': 'pregnancy rate', 'timeFrame': '14 days after embryos transfer', 'description': 'β-hCG (serum hCG test) will be checked 14 days after embryos transfer'}]}, 'oversightModule': {'oversightHasDmc': True}, 'conditionsModule': {'keywords': ['infertility ICSI OHSS Calcium Dobesilate Cabergoline'], 'conditions': ['Infertility']}, 'descriptionModule': {'briefSummary': 'The purpose of this study is to compare the effect of oral Calcium Dobesilate to oral Cabergoline in the prevention of ovarian hyperstimulation syndrome (OHSS) in high-risk women underwent intracytoplasmic sperm injection (ICSI).', 'detailedDescription': 'Two hundred and twenty women at risk of ovarian hyperstimulation syndrome during ICSI cycles will be randomly scheduled into two equal groups. In group A, (Calcium Dobesilate group), 1 cap / 8 hs Doxium ( 500mg) will be given at day of HCG injection and for 21 days; while in group B (Cabergoline group), 1 tab/day Cabergoline( 0.5 mg) will be given at day of HCG injection and for 8 days.'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT'], 'maximumAge': '44 Years', 'minimumAge': '22 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Patients enrolled in the study were infertile women undergoing ICSI with one of the following criteria: previous episodes of OHSS, polycystic ovaries (i.e., \\> 24 antral follicles present on baseline ultrasound examination), high AMH (\\> 3.0 ng/mL), large number of small follicles (8 to 12 mm) seen on ultrasound during ovarian stimulation, high s.E2 at hCG trigger (E2 \\>3000 pg/ml or rapidly rising s.E2), presence of \\> 20 follicles by ultrasound on day of retrieval or large number of oocytes retrieved (\\> 20).\n\nExclusion Criteria:\n\n* None'}, 'identificationModule': {'nctId': 'NCT02271360', 'briefTitle': 'Calcium Dobesilate Versus Cabergoline for Prevention of Ovarian Hyperstimulation Syndrome', 'organization': {'class': 'OTHER', 'fullName': 'Benha University'}, 'officialTitle': 'Calcium Dobesilate Versus Cabergoline for Prevention of Ovarian Hyperstimulation Syndrome', 'orgStudyIdInfo': {'id': 'khalid-ahmed 7'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'group A', 'description': 'In group A, (Calcium Dobesilate group), 1 cap / 8 hs Calcium Dobesilate ( 500mg) will be given from at day of HCG injection and for 21 days.', 'interventionNames': ['Drug: Calcium Dobesilate']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'group B', 'description': 'while in group B (Cabergoline group), 1 tab/day Cabergoline(Dostinex)( 0.5 mg) will be givenat day of HCG injection and for 8 days .', 'interventionNames': ['Drug: Cabergoline']}], 'interventions': [{'name': 'Calcium Dobesilate', 'type': 'DRUG', 'otherNames': ['doxium'], 'description': '1 cap / 8 hs Calcium Dobesilate ( 500mg) will be given at day of HCG injection and for 21 days', 'armGroupLabels': ['group A']}, {'name': 'Cabergoline', 'type': 'DRUG', 'otherNames': ['Dostinex'], 'description': '1 tab/day Cabergoline( 0.5 mg) will be given at day of HCG injection and for 8 days', 'armGroupLabels': ['group B']}]}, 'contactsLocationsModule': {'locations': [{'zip': '13518', 'city': 'Banhā', 'state': 'El Qualyobia', 'country': 'Egypt', 'facility': 'Benha univesity hospital', 'geoPoint': {'lat': 30.45977, 'lon': 31.1842}}], 'overallOfficials': [{'name': 'khalid mohamed, MD', 'role': 'STUDY_CHAIR', 'affiliation': 'lecturer of ob/gyn'}, {'name': 'ahmed saad, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'lecturer of ob/gyn'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Benha University', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'lecturer of ob/gyn', 'investigatorFullName': 'khalid abd aziz mohamed', 'investigatorAffiliation': 'Benha University'}}}}