Nctid:
NCT00000929
Payload:
{"hasResults"=>false, "derivedSection"=>{"miscInfoModule"=>{"versionHolder"=>"2024-09-05"}, "conditionBrowseModule"=>{"meshes"=>[{"id"=>"D000015658", "term"=>"HIV Infections"}], "ancestors"=>[{"id"=>"D000086982", "term"=>"Blood-Borne Infections"}, {"id"=>"D000003141", "term"=>"Communicable Diseases"}, {"id"=>"D000007239", "term"=>"Infections"}, {"id"=>"D000015229", "term"=>"Sexually Transmitted Diseases, Viral"}, {"id"=>"D000012749", "term"=>"Sexually Transmitted Diseases"}, {"id"=>"D000016180", "term"=>"Lentivirus Infections"}, {"id"=>"D000012192", "term"=>"Retroviridae Infections"}, {"id"=>"D000012327", "term"=>"RNA Virus Infections"}, {"id"=>"D000014777", "term"=>"Virus Diseases"}, {"id"=>"D000091662", "term"=>"Genital Diseases"}, {"id"=>"D000091642", "term"=>"Urogenital Diseases"}, {"id"=>"D000007153", "term"=>"Immunologic Deficiency Syndromes"}, {"id"=>"D000007154", "term"=>"Immune System Diseases"}], "browseLeaves"=>[{"id"=>"M10283", "name"=>"Infections", "relevance"=>"LOW"}, {"id"=>"M6368", "name"=>"Communicable Diseases", "relevance"=>"LOW"}, {"id"=>"M18250", "name"=>"HIV Infections", "asFound"=>"HIV Infections", "relevance"=>"HIGH"}, {"id"=>"M3522", "name"=>"Acquired Immunodeficiency Syndrome", "relevance"=>"LOW"}, {"id"=>"M2593", "name"=>"Blood-Borne Infections", "relevance"=>"LOW"}, {"id"=>"M15558", "name"=>"Sexually Transmitted Diseases", "relevance"=>"LOW"}, {"id"=>"M17933", "name"=>"Sexually Transmitted Diseases, Viral", "relevance"=>"LOW"}, {"id"=>"M18640", "name"=>"Lentivirus Infections", "relevance"=>"LOW"}, {"id"=>"M15026", "name"=>"Retroviridae Infections", "relevance"=>"LOW"}, {"id"=>"M17522", "name"=>"Virus Diseases", "relevance"=>"LOW"}, {"id"=>"M15149", "name"=>"RNA Virus Infections", "relevance"=>"LOW"}, {"id"=>"M2876", "name"=>"Genital Diseases", "relevance"=>"LOW"}, {"id"=>"M2875", "name"=>"Urogenital Diseases", "relevance"=>"LOW"}, {"id"=>"M16355", "name"=>"Syndrome", "relevance"=>"LOW"}, {"id"=>"M10199", "name"=>"Immunologic Deficiency Syndromes", "relevance"=>"LOW"}, {"id"=>"M10200", "name"=>"Immune System Diseases", "relevance"=>"LOW"}], "browseBranches"=>[{"name"=>"Infections", "abbrev"=>"BC01"}, {"name"=>"All Conditions", "abbrev"=>"All"}, {"name"=>"Symptoms and General Pathology", "abbrev"=>"BC23"}, {"name"=>"Urinary Tract, Sexual Organs, and Pregnancy Conditions", "abbrev"=>"BXS"}, {"name"=>"Immune System Diseases", "abbrev"=>"BC20"}]}, "interventionBrowseModule"=>{"meshes"=>[{"id"=>"D000017137", "term"=>"Nonoxynol"}], "ancestors"=>[{"id"=>"D000013089", "term"=>"Spermatocidal Agents"}, {"id"=>"D000000988", "term"=>"Antispermatogenic Agents"}, {"id"=>"D000045505", "term"=>"Physiological Effects of Drugs"}, {"id"=>"D000003271", "term"=>"Contraceptive Agents, Female"}, {"id"=>"D000003270", "term"=>"Contraceptive Agents"}, {"id"=>"D000012102", "term"=>"Reproductive Control Agents"}, {"id"=>"D000003272", "term"=>"Contraceptive Agents, Male"}], "browseLeaves"=>[{"id"=>"M4214", "name"=>"Anti-Infective Agents", "relevance"=>"LOW"}, {"id"=>"M251802", "name"=>"Imidacloprid", "relevance"=>"LOW"}, {"id"=>"M19451", "name"=>"Nonoxynol", "asFound"=>"Tampa", "relevance"=>"HIGH"}, {"id"=>"M15888", "name"=>"Spermatocidal Agents", "relevance"=>"LOW"}, {"id"=>"M6494", "name"=>"Contraceptive Agents", "relevance"=>"LOW"}, {"id"=>"M6495", "name"=>"Contraceptive Agents, Female", "relevance"=>"LOW"}, {"id"=>"M6496", "name"=>"Contraceptive Agents, Male", "relevance"=>"LOW"}], "browseBranches"=>[{"name"=>"Anti-Infective Agents", "abbrev"=>"Infe"}, {"name"=>"All Drugs and Chemicals", "abbrev"=>"All"}, {"name"=>"Reproductive Control Agents", "abbrev"=>"Repr"}]}}, "protocolSection"=>{"designModule"=>{"phases"=>["PHASE1"], "studyType"=>"INTERVENTIONAL", "designInfo"=>{"primaryPurpose"=>"PREVENTION"}, "enrollmentInfo"=>{"count"=>70}}, "statusModule"=>{"overallStatus"=>"COMPLETED", "expandedAccessInfo"=>{"hasExpandedAccess"=>false}, "statusVerifiedDate"=>"2021-10", "completionDateStruct"=>{"date"=>"1999-07", "type"=>"ACTUAL"}, "lastUpdateSubmitDate"=>"2021-10-27", "studyFirstSubmitDate"=>"1999-11-02", "studyFirstSubmitQcDate"=>"2001-08-30", "lastUpdatePostDateStruct"=>{"date"=>"2021-10-29", "type"=>"ACTUAL"}, "studyFirstPostDateStruct"=>{"date"=>"2001-08-31", "type"=>"ESTIMATED"}}, "oversightModule"=>{"oversightHasDmc"=>true}, "conditionsModule"=>{"keywords"=>["Sexual Partners", "Homosexuality, Male", "Anti-Infective Agents", "Patient Compliance", "Nonoxynol", "Rectum"], "conditions"=>["HIV Infections"]}, "descriptionModule"=>{"briefSummary"=>"The purpose of this study is to see if it is safe and acceptable for homosexual male couples, where both partners have the same HIV status, to use Advantage 24 during anal intercourse. Advantage 24 is a spermicide (a chemical that kills sperm).\n\nMuch research and development is being done with chemicals that can be controlled by the receptive partner to prevent the spread of HIV and other sexually transmitted diseases (STDs). Advantage 24 currently is used in the vagina as a form of birth control. The safety of Advantage 24 is particularly important for HIV-positive men because they have a greater chance of serious reaction to Advantage 24 due to other HIV-related conditions.", "detailedDescription"=>"Chemical barriers which can be controlled by the receptive partner to prevent transmission of HIV and other sexually transmitted diseases (STDs) are among the highest priorities for research and development. Advantage 24 is a contraceptive gel containing nonoxynol-9 (N-9). This study provides information on the safety of N-9 in a bioadhesive gel formulated for use by MSM during anal intercourse. Safety is assessed for both HIV-positive and HIV-negative men because HIV-positive men may be at increased risk for toxicity due to other HIV-related conditions.\n\nParticipants are divided into 4 cohorts depending on their serostatus and whether they are the insertive or receptive partner. Participants apply Advantage 24 once or twice a day for 5 weeks and 4 times a day for the sixth week. Check-in visits, which include a genital exam, are performed at Weeks 1, 2, 4, 5, and 7. More complete physical evaluations, including anoscopy for receptive partners and blood tests, are performed at Weeks 3, 6, and 8."}, "eligibilityModule"=>{"sex"=>"MALE", "stdAges"=>["ADULT", "OLDER_ADULT"], "minimumAge"=>"18 years", "healthyVolunteers"=>true, "eligibilityCriteria"=>"Exclusion Criteria\n\nCo-existing Condition:\n\nParticipants with the following symptoms or conditions are excluded:\n\n* Positive HSV-2 serology (HIV-negative participants only).\n* Positive syphilis by Venereal Disease Research Laboratory (VDRL) serology and Fluorescent Treponemal Antibody (FTA) or Microhemagglutination Assay (MHA).\n\nReceptive partners with the following additional symptoms or conditions are excluded:\n\n* Rectal gonorrhea or chlamydia by culture.\n* Active rectal inflammation, ulceration, or fissures.\n\nInsertive partners with the following additional symptoms or conditions are excluded:\n\n* Penile or urethral irritation, rashes, or lesions.\n* Penile or scrotal piercing.\n\nConcurrent Medication:\n\nExcluded for receptive partners:\n\n-\n\nAnticoagulant, including warfarin and heparin.\n\nParticipants with the following prior conditions are excluded:\n\n* Sensitivity or irritative symptoms when using N-9 or when exposed to latex.\n* Three or more Herpes Simplex 2 Virus (HSV-2) outbreaks within 12 months prior to screening (HIV-positive participants only).\n* One or more HSV-2 outbreaks within 6 months prior to screening (HIV-positive participants only).\n\nReceptive partners with the following additional prior conditions are excluded:\n\n* Diagnosed inflammatory bowel disease, ulcerative colitis, Crohn's disease, or rectal malignancy.\n* Diagnosed bleeding disorder, including hemophilia and thrombocytopenia.\n* Rectal surgery including fistulectomy.\n* Prosthetic heart valve or diagnosis of a valvular abnormality.\n* Hemorrhoidectomy within 6 months prior to screening.\n* Rectal burning, tenesmus, bleeding, or irritation in the week prior to screening.\n* Diarrhea (more than 3 stools per day) in the week prior to screening.\n* Use of rectally-inserted sex toys, practiced receptive fisting, or rectal douching in the week prior to screening.\n\nInsertive partners with the following additional prior conditions are excluded:\n\nUrethral burning or discharge in the week prior to screening.\n\nPrior Medication:\n\nExcluded for receptive partners:\n\nUse of laxatives in the week prior to screening.\n\nParticipants meet the following criteria:\n\n* HIV-negative or HIV-positive; participant's partner must be the same serostatus.\n* Plan to have anal intercourse only with the study partner for the duration of the study. During all episodes in which Advantage 24 is used, one partner is exclusively insertive and the other partner is exclusively receptive.\n* Sexual partner of at least 3 months is eligible and agrees to participate.\n* Agree to use non-N-9 lubricant and condoms for all episodes of anal intercourse.\n* Avoid use of Advantage 24 for purposes other than specified by the protocol.\n\nReceptive partners meet the following additional criteria:\n\n* Plan to have receptive anal intercourse with the study partner with Advantage 24 applied rectally, and using N-9 lubricant and condoms, at the couple's usual frequency (at least 3 times per week).\n* Agree to apply the specified amount of Advantage 24 daily to the rectum.\n* Avoid use of laxatives, use of rectally-inserted sex toys, receptive fisting, and rectal douching.\n\nInsertive partners meet the following additional criteria:\n\n* Plan to have insertive anal intercourse with the study partner with Advantage 24 applied to the glans of the penis, and using non-N-9 lubricant and condoms, at the couple's usual frequency (at least 3 times per week).\n* Agree to apply the specified amount of Advantage 24 daily to the penis."}, "identificationModule"=>{"nctId"=>"NCT00000929", "briefTitle"=>"A Study of the Effects of Advantage 24 on the Rectum", "organization"=>{"class"=>"NIH", "fullName"=>"National Institute of Allergy and Infectious Diseases (NIAID)"}, "officialTitle"=>"Phase I Rectal Microbicide Study", "orgStudyIdInfo"=>{"id"=>"HIVNET 008"}, "secondaryIdInfos"=>[{"id"=>"11715", "type"=>"REGISTRY", "domain"=>"DAIDS ES"}]}, "armsInterventionsModule"=>{"interventions"=>[{"name"=>"Nonoxynol-9", "type"=>"DRUG"}]}, "contactsLocationsModule"=>{"locations"=>[{"zip"=>"98104", "city"=>"Seattle", "state"=>"Washington", "country"=>"United States", "facility"=>"Univ of Washington", "geoPoint"=>{"lat"=>47.60621, "lon"=>-122.33207}}], "overallOfficials"=>[{"name"=>"Connie Celum", "role"=>"STUDY_CHAIR"}, {"name"=>"Susan Buchbinder", "role"=>"STUDY_CHAIR"}]}, "sponsorCollaboratorsModule"=>{"leadSponsor"=>{"name"=>"National Institute of Allergy and Infectious Diseases (NIAID)", "class"=>"NIH"}, "responsibleParty"=>{"type"=>"SPONSOR"}}}}