Bausch Health Companies Inc.: all 534 studies

Page 5 of 6. Open to participants first (17), then studies with results posted, then the rest; newest registration first within each.

• Open-Label Treatment Extension of Protocol MNTX 301CompletedNCT01367600Phase 3
• Safety and Gastrointestinal Effects of Intravenous MethylnaltrexoneCompletedNCT01367587Phase 2
• Methylnaltrexone in Patients With Opioid-Induced Bowel DysfunctionCompletedNCT01367574Phase 2
• Naloxone and Intravenous Methylnaltrexone Effects on Bladder FunctionCompletedNCT01367561Phase 1
• Intravenous (IV) Methylnaltrexone (MNTX) in the Prevention of Post-Operative IleusCompletedNCT01367548Phase 2
• Effects of MNTX on CYP450 2D6 in Metabolizers of DextromethorphanCompletedNCT01367535Phase 1
• Pharmacokinetics, Safety, and Tolerability of Methylnaltrexone in Volunteers With Impaired Hepatic FunctionCompletedNCT01367522Phase 1
• Pharmacokinetics, Safety, and Tolerability of Methylnaltrexone (MNTX) in Subjects With Impaired Renal FunctionCompletedNCT01367509Phase 1
• Pharmacokinetics and Bioavailability of Single Subcutaneous Doses of Methylnaltrexone Versus Intravenous DoseCompletedNCT01367496Phase 1
• Study of the Pharmacokinetics of Intravenous Administered 14C-MNTXCompletedNCT01367483Phase 1
• Effect of Cimetidine on the Single-Dose PK of IV- Administered MNTXCompletedNCT01366378Phase 1
• Study of Pharmacokinetics, Safety and Tolerability of Intravenous Methylnaltrexone BromideCompletedNCT01366365Phase 1
• Pharmacokinetics and Bioavailability Comparison of Two Different Formulations of MNTX TabletsCompletedNCT01366352Phase 1
• Tolerance and Pharmacokinetics Study of MNTX TabletsCompletedNCT01366339Phase 1
• Evaluate the Pharmacokinetics (PK) of Methylnaltrexone (MNTX) in Healthy Adult SubjectsCompletedNCT01366326Phase 1
• Effect of Methylnaltrexone (MNTX) on Electrocardiogram (ECG) Parameters and Cardiac RepolarizationCompletedNCT01363323Phase 1
• Topical Antifungal Treatment for Tinea CrurisCompletedNCT01342315Phase 3
• Safety and Efficacy Study to Evaluate the Treatment of Both Near and Distance Vision in a Simultaneous Laser ProcedureCompletedNCT01322919Phase 3
• Evaluation of a Photopneumatic System for the Treatment of AcneCompletedNCT01257555
• Combination Treatment for Moderate to Severe AcneCompletedNCT01206348Phase 4
• A Dose-Ranging Study Evaluating the Safety and Efficacy of IDP-107 in Patients With Acne VulgarisCompletedNCT01194375Phase 2
• Long Term Observation of Patient Satisfaction Post INTRACOR Treatment Based on Patient Perception and Diagnostic DataCompletedNCT01164358
• A Study Comparing the Safety and Tolerability of Two Doses of Fipamezole in Adult Patients With Parkinson's DiseaseCompletedNCT01149811
• A Study of Safety and Tolerability of Fipamezole in Adult Subjects With Parkinson's Disease Who Are Receiving LevodopaCompletedNCT01140841
• An Extension Trial to Evaluate Long-term Safety of SABER™-Bupivacaine for Pain Following Shoulder SurgeryCompletedNCT01139866
• A Study of the Effectiveness and Safety of Tetrabenazine MR in Pediatric Subjects With Tourette's SyndromeWithdrawnNCT01133353Phase 2
• Corneal Endothelial Cell Density Changes In Healthy Subjects, When Administered ISV-403 for 5 DaysCompletedNCT01120418Phase 1
• Study of the Efficacy and Safety of Bupivacaine TTS Patch in Patients With Chronic Low Back PainCompletedNCT01096966Phase 2
• Evaluation of Corneal Endothelial Cell Density in Subjects Who Have Had a Fluocinolone Acetonide ImplantCompletedNCT01060787
• Intrastromal Presbyopia Correction by Means of a Femtosecond LaserCompletedNCT01025050Phase 3
• Safety and Efficacy of Topical IDP-108 Versus Vehicle in Patients With OnychomycosisCompletedNCT01008033Phase 3
• The Safety and Efficacy of Topical IDP-108 Versus Vehicle in Patients With OnychomycosisCompletedNCT01007708Phase 3
• Study to Evaluate Efficacy and Safety in Male Subjects With Premature EjaculationTerminatedNCT00983736Phase 3
• Study to Evaluate Efficacy and Safety in Males Subjects With Premature EjaculationTerminatedNCT00983151Phase 3
• Multicenter Evaluation of Safety and Effectiveness of Presbyopic LASIK for HyperopesCompletedNCT00910403Phase 3
• Concentration of Besifloxacin, Gatifloxacin, and Moxifloxacin in Human Conjunctiva After Topical InstillationCompletedNCT00905762Phase 1
• Indomethacin Eyedrops Compared With Ketorolac Eyedrops for Ocular Inflammation Following Cataract SurgeryCompletedNCT00904904Phase 4
• Biopsy Study for Sculptra (Poly-L-Lactic Acid)CompletedNCT00869687Not applicable
• Study Evaluating Safety & Efficacy of Subcutaneous Methylnaltrexone on Opioid-Induced Constipation in Cancer SubjectsWithdrawnNCT00858754Phase 4
• Evaluation of the Safety & Effectiveness of the Bausch & Lomb AKREOS® TL Intraocular LensCompletedNCT00838045Phase 4
• Safety and Effectiveness of the Akreos Toric Intraocular Lens.CompletedNCT00825513Phase 4
• Safety and Effectiveness Study of the AcuFocus Corneal Inlay ACI 7000PDT in PresbyopesCompletedNCT00819299Not applicable
• Evaluation of the Safety and Effectiveness of the Akreos MI Five-0 Intraocular Lens.TerminatedNCT00804726Not applicable
• Injectable POLY-L-Lactic Acid for Treatment of Hill and Valley Acne ScarringCompletedNCT00795327Not applicable
• A Dose-Ranging Study Evaluating the Safety and Efficacy of IDP-108 in Patients With OnychomycosisCompletedNCT00777868Phase 2
• Comparative Study of the Wearing Satisfaction of Two Soft Contact Lens Designs.CompletedNCT00768885Not applicable
• Mesalamine Pellet to Maintain Remission of Mild to Moderate Ulcerative ColitisCompletedNCT00767728Phase 3
• A Study to Determine How Long Restylane® Will Last After Initial Treatment With 2 Different Re-treatment Schedules.CompletedNCT00765583Phase 4
• Mesalamine Pellet Formulation to Maintain Remission of Mild to Moderate Ulcerative ColitisCompletedNCT00744016Phase 3
• Open-Label Study to Evaluate the Effect of Rifaximin on Midazolam in Normal Healthy VolunteersCompletedNCT00743912Phase 1
• Ocular Responses to Short and Long-term Lens WearCompletedNCT00722891Not applicable
• A Clinical Study Evaluating the Safety and Efficacy of IDP-115 in Patients With RosaceaCompletedNCT00667173Phase 2
• A Clinical Study Evaluating the Safety and Efficacy of IDP-107 in Patients With Acne VulgarisCompletedNCT00666900Phase 2
• A Clinical Study Evaluating the Safety and Efficacy of IDP-110 in Patients With Acne VulgarisCompletedNCT00664248Phase 3
• A Clinical Trial Evaluating the Safety and Efficacy of IDP-110 in Patients With Acne VulgarisCompletedNCT00663286Phase 3
• Effect of Tetrix on Alleviation of Burning,Itching Associated With Lesions of Contact DermatitisCompletedNCT00646867Not applicable
• Study to Determine if Tetrix Cream is Removed From the Hands by Gentle Washing With Soap and WaterCompletedNCT00644436Not applicable
• Evaluation of Tetrix Cream as a Protective Barrier Against Injurious MaterialsCompletedNCT00643630Not applicable
• Evaluation of Tetrix Cream in the Healing of Injured Skin in Subjects With Contact DermatitisCompletedNCT00643214Not applicable
• Compassionate Use Study of Pergolide in Patients With Parkinson's DiseaseNo longer availableNCT00624741
• PK Study of Encapsulated Mesalamine Granules in Healthy VolunteersCompletedNCT00622375Phase 1
• A Study to Determine the Safety and Efficacy of Atralin (Tretinoin 0.05%) Gel for the Treatment of RosaceaCompletedNCT00621218Phase 2
• Study to Determine the Phototoxity of Atralin (Tretinoin) Gel, 0.05%CompletedNCT00604032Phase 1
• Clinical Evaluation of the Photoallergy Potential of Atralin GelCompletedNCT00603772Phase 1
• Safety and Efficacy of Intravitreal Fluocinolone Acetonide Implants in Patients With Diabetic Macular EdemaCompletedNCT00576459Phase 2
• 10 Year Registry of Children (Ages 2-17 Years) With Eczema That Have Used PimecrolimusActive, not recruitingNCT00568997
• Loteprednol Etabonate Opthalmic Suspension for the Treatment of Dry EyeCompletedNCT00560638Phase 2
• Ocular Tolerance and Intraocular Pressure (IOP) Effects of Zylet Versus TobradexCompletedNCT00532961Phase 4
• Study Evaluating Oral MOA-728 in Subjects on Methadone TherapyWithdrawnNCT00505583Phase 1
• Efficacy of Fluocinolone Acetonide Intravitreal Implant in Diabetic Macular EdemaCompletedNCT00502541Phase 2/3
• A Single-Center, Open-Label, Exploratory Study of the Volumizing Effect of SCULPTRA Measured by Three Dimensional Digital Surface ImagingCompletedNCT00487474
• Open Label, Safety Study of EN3270 in Patients With Moderate to Severe Non-malignant, Chronic PainCompletedNCT00485225Phase 2
• Study of a Bupivacaine Patch (Eladur™) to Treat Post- Herpetic NeuralgiaCompletedNCT00478179Phase 2
• Safety and Efficacy of Fluocinolone Acetonide Intravitreal Implant vs Standardized TherapyCompletedNCT00468871Phase 2/3
• Study Evaluating the Safety and Tolerability of a New Intravenous Formulation of MOA-728 in Healthy SubjectsCompletedNCT00464802Phase 1
• Diarrhea Predominant Irritable Bowel Syndrome in FemalesCompletedNCT00461526Phase 2
• Safety and Efficacy of Fluocinolone Acetonide Intravitreal ImplantTerminatedNCT00456482Phase 2/3
• Study Evaluating MOA-728 in Subjects on Stable Methadone MaintenanceCompletedNCT00447811Phase 1
• Zylet vs TobraDex in BlepharokeratoconjunctivitisCompletedNCT00447577Phase 4
• Canadian Aesthetic Experience With Sculptra TherapyCompletedNCT00447551Phase 4
• DL6049 Versus Cosmoplast in the Treatment of Nasolabial Fold Wrinkles, Long Term Follow-upCompletedNCT00444353Phase 3
• DL6049 vs CosmoPlast in the Treatment of Nasolabial Fold WrinklesCompletedNCT00444210Phase 3
• Double-Blind, Double-Dummy, 2-Period Crossover of a 20-Minute Versus a 4-hour IV of MOA-728 in Stable Methadone SubjectsCompletedNCT00444158Phase 1
• Study Evaluating the Effects of MOA-728 on Cardiac Repolarization in Healthy SubjectsCompletedNCT00434395Phase 1
• Study Evaluating MOA-728 Administered in Healthy MenWithdrawnNCT00427258Phase 1
• Efficacy and Safety of Topical Bromfenac Ophthalmic Solution vs. Placebo in Subjects With Allergic ConjunctivitisCompletedNCT00423007Phase 3
• Balsalazide Disodium vs. Mesalamine in Mildly to Moderately Active Ulcerative ColitisCompletedNCT00408174Phase 3
• Systemic Pharmacokinetics of BOL-303224-ACompletedNCT00407589Phase 1
• Safety and Efficacy of Fluocinolone Acetonide Intravitreal ImplantsCompletedNCT00407082Phase 2/3
• Study of Methylnaltrexone (MNTX) for the Relief of ConstipationCompletedNCT00402038Phase 3
• A a Single Dose Efficacy Study in Inducing Laxation in Advance Illness PatientsCompletedNCT00401362Phase 3
• Comparisons Of The Bioavailability And Pharmacodynamics Of Various Formulations Of MOA-728 In Subjects On MethadoneCompletedNCT00398502Phase 1
• Bioequivalence Study in Healthy VolunteersCompletedNCT00387985Phase 1
• Dose Ranging Study in Healthy Methadone Maintenance SubjectsCompletedNCT00387491Phase 1
• Study Evaluating IV Methylnaltrexone for the Treatment of Post Operative IleusCompletedNCT00387309Phase 3
• A Study Of The Safety And Effectiveness Of A New Treatment For Allergic ConjunctivitisWithdrawnNCT00375596Phase 2
• Effect of Adjunctive Treatment With Arestin on the Subgingival Microflora in Patients With Moderate to Advanced PeriodontitisCompletedNCT00371332Phase 3
• Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye SyndromeCompletedNCT00370747Phase 2
• Study Evaluating Oral MOA-728 for the Treatment of Opioid-Induced Bowel Dysfunction (OIBD) in Subjects With Chronic Non-Malignant PainCompletedNCT00366431Phase 2
• A Study to Investigate the Safety and Effectiveness of Aspheric Laser Refractive Surgery Treatments for MyopiaCompletedNCT00365677Not applicable

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