Clinical Trials in Atlanta

Showing 19381-19400 of 19,805 trials

Fetal Alcohol Syndrome: Socio-Cognitive Habilitation

NCT00164229

Comprehensive evaluation (geneticist, psychologist, social worker, education specialist, others as indicated) to determine individual needs and treatment plan. Referrals for specific services (e.g., OT, counseling, medications, etc) will be to clinicians within the families' own communities. All families will receive evaluation, parent education/advocacy, and learning readiness program. Only the intervention group will receive the math intervention.

Fetal Alcohol Syndrome

Centers for Disease Control and Prevention100 participantsStarted Oct 2001

Atlanta, Georgia, United States

COMPLETEDPhase 3< 1 mile

Study to Establish Bioequivalence of ReFacto AF (BDDrFVIII) With Advate (FLrFVIII) in Hemophilia A

NCT00141843

The study will consist of two parts: a safety and efficacy period in which all subjects will participate and a pharmacokinetic analysis period, in which 30 eligible subjects will participate to compare ReFacto AF and Advate bioequivalency and safety and efficacy of ReFacto AF in patients with Hemophilia A.

Hemophilia A

Wyeth is now a wholly owned subsidiary of Pfizer100 participantsStarted Jul 2005

Phoenix, Arizona, United States • Sacramento, California, United States • San Diego, California, United States +38 more locations

Fetal Alcohol Syndrome: Socio-Cognitive Habilitation

Study to Establish Bioequivalence of ReFacto AF (BDDrFVIII) With Advate (FLrFVIII) in Hemophilia A

Find Trials by Condition in Atlanta

Study to Evaluate the Effect of SLV320 in Addition to Chronic Furosemide Treatment on Renal Function in Subjects With Congestive Heart Failure and Impaired Renal Function

Safety, Tolerability and Efficacy of the Transdermal System in Elderly Subjects With Major Depression

The Efficacy of ESTRATEST® Tablets in Relieving Menopausal Symptoms in Estrogenized, Hysterectomized Postmenopausal Women

Single Tablet Regimen (STR) Simplification Study for HIV-1 Infected Patients

Safety and Efficacy Study of Brimonidine in Patients With Glaucoma or Ocular Hypertension

Dronabinol Versus Placebo in Treatment and Prevention of Highly Active Anti-Retroviral Therapy (HAART)-Related Nausea and Vomiting

Dronabinol Versus Standard Ondansetron Antiemetic Therapy in Preventing Delayed-Onset Chemotherapy-Induced Nausea and Vomiting

A Clinical Trial Assessing the Impact of the Availability of Inhaled Insulin on Glucose Control

PK Study of Tacrolimus and Cyclosporine When Co-Administered With Adefovir Dipivoxil in Post-Liver Transplant Patients

SLV 308 and Pramipexole for Treatment of Patients With Early Parkinson Disease

Study to Compare the Overall Survival of Patients Receiving INGN 201 (Study Drug) With Patients Receiving Methotrexate

The OMEGA Study: Use of Eye Drops to Treat Geographic Atrophy Associated With Age-Related Macular Degeneration (Dry AMD)

Sapropterin Expanded Access Program

An Open Label Study of a Peptide Vaccine in Patients With Stage III Colon Cancer

Phase 3 Safety and Efficacy Study of I.V. Iclaprim v Linezolid in cSSSI (ASSIST-1)

Study of Individualized Amonafide to Treat Prostate Cancer

Study of Safety and Tolerability of Intravenous CRS-100 in Adults With Carcinoma and Liver Metastases

Immunotherapy With BHT-3009 Alone or Combined With Atorvastatin in Patients With Multiple Sclerosis