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23451 Madison St. #290
Torrance, CA 90505
(310) 375-1246
fax (310) 375-0590
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James A. Sattler, M.D.
Education
| 1982-1984 |
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Gastroenterology / Hepatology Fellow: Kaiser Foundation Hospital - Los Angeles, California |
| 1980-1982 |
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Residency: Kaiser Foundation Hospital - Los Angeles, California |
| 1979-1980 |
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Internship: Kaiser Foundation Hospital - Los Angeles, California |
| 1978-1979 |
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Doctor of Medicine: University of Southern California |
| 1975-1978 |
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Bachelor of Arts - Psychology, University of California, Berkeley |
Honors
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Phi Beta Kappa, Alpha Omega Alpha |
| 1988 |
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Internist of the Year
Southern California Permanente Medical Group
Los Angeles Medical Center |
Certifications
| American Board of Internal Medicine, 1982 |
| American Board of Internal Medicine, Gastroenterology Subspecialty, 1985 |
Hospital Affiliations
| 1999-Present |
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HealthSouth, Surgery Center of South Bay
Torrance, California |
| 1990-Present |
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Active Affiliation, Little Company of Mary
Torrance, California |
| 1990-Present |
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Active Affiliation, Torrance Memorial Medical Center
Torrance, California |
| 1990-Present |
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Active Affiliation, San Pedro Hospital
San Pedro, California |
Professional Affiliations
| Member, American College of Physicians |
| Member, Southern California Society of Gastrointestinal Endoscopy |
| Associate Member, American Gastroenterology |
Work Experience
| 2002-Present |
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Medical Director - Endoscopy Center at Skypark, Torrance, CA |
| 1999-Present |
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Western Clinical Research, Inc., Torrance, CA |
| 1990-Present |
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Gastroenterologist Partner, Digestive Care Consultants |
| 1986-1989 |
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Assistant Director of the Adult Liver Transplantation Committee, Permanente Medical Group, Southern California Region, Los Angeles, California |
| 1986-1989 |
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Assistant Director, Internal Medicine - Kaiser Foundation Hospital, Los Angeles, California |
| 1984-1989 |
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Internist and Gastroenterologist - Kaiser Foundation Hospital, Los Angeles, California |
Academic Appointments
| 1984-1989 |
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Clinical Instructor of Medical Students, Interns - Kaiser Foundation Hospital, Los Angeles, California |
| 1984-1989 |
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Clinical Instructor of Gastroenterologist Fellows - Kaiser Foundation Hospital, Los Angeles, California |
Research Activities
- A randomized, double-blind, placebo controlled, multicenter 2-week pilot study to evaluate the efficacy, safety and tolerability of XXX (25 and 100 mg bid) given orally in female patients with Irritable Bowel Syndrome with diarrhea (IBS-D)
- A 6-week, Randomized, Double-blind, Placebo-controlled, Multicenter Study, to Assess the Efficacy and Safety of XXXX (6mg BID) and Placebo in Female Patients with Dyspepsia
- A Multicenter, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Low-Dose XXXX in Male Patients with Irritable Bowel Syndrome
- Safety, Tolerance and Efficacy of Treatment with Subcutaneous XXX in Subjects With Steroid-Dependent Crohn's Disease
- A Randomized, Open-Label, Multicenter, Efficacy, Tolerability and Safety Study of XXX Vs. XXX in Interferon and Ribavirin Treatment Naïve Patients with Chronic Hepatitis C Infection
- A 24 Week Randomized, Open Label Study of Health Care Resource Use and Quality of Life and Productivity with XXX 1 mg. Twice Daily versus Traditional Therapy in Females With Non-Constipated Irritable Bowel Syndrome
- A Twelve-Week, Randomized, Double-Blind, Placebo-Controlled Study of XXX In Females With Non-Constipated Irritable Bowel Syndrome
- Double-Blind, Placebo-Controlled Long-Term Extension Study to Evaluate the Nine Month Safety Profile of XXX in Non-Constipated IBS Patients
- Double-Blind, Placebo-Controlled, Randomized, Multicenter, Parallel-Group Dose-Ranging Study To Investigate The Efficacy And Safety Of XXX In Non-Constipated Patients With Irritable Bowel Syndrome
- A Twelve-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging, Phase II Study to Assess The Clinical Efficacy of XXX in Male Subjects with Irritable Bowel Syndrome
- A Double-Blind, Randomized, Placebo-Controlled, Phase II Clinical Trial Of XXX For Treatment Of Non-Ulcer Dyspepsia In Patients Without Helicobacter Pylori
- A Randomized, Double-Blind, Active Controlled, Parallel Group, Multicenter Study to Evaluate The Efficacy And Safety Of XXX and XXX In Patients With Active, Mild To Moderate Ulcerative Colitis
- Dose-Finding Safety And Efficacy Study Of XXX Treatment To Reduce The Occurrence Of Sporadic Adenomatous Colorectal Polyps AT One Year In Subjects With Intermediate Risk Of Developing Polyps And Colorectal Cancer
- Prevention Of Sporadic Colorectal Adenomas With XXX
- A Comparative Efficacy And Safety Study Of XXX Versus XXX (150 mg bid) For The Healing Of NSAID Associated Gastric Ulcers When Daily NSAID Use Is Continued
- A Comparative Efficacy And Safety Study Of XXX Versus Placebo For The Prevention Of Gastric Ulcers Associated With Daily NSAID use In Patients At Risk
- A Randomized, Double-Blind Trial Comparing The Early Profile Of Heartburn Relief Associated With XXX 20mg daily Versus XXX, 20mg Once Daily In Gastroesophageal Reflux Disease Patients With An Acute Or Documented History Of Erosive Esophagitis
- A Double-Blind, Placebo-Controlled Trial Of XXX Tablets, 20mg Once Daily In The Treatment Of Subjects Without Erosive Esophagitis And Have Symptoms Of Chronic Gastroesophageal Reflux Disease (GERD)
- A Phase III Study Of The Safety And Antiviral Activity Of XXX In Adults With Chronic Hepatitis B Infection Who Are Positive For Hepatitis B E Antigen
- A Preliminary Assessment Of Safety And Antiviral Activity Of Open-Label XXX Plus XXX Therapy In Subjects With Chronic Hepatitis B Who Have Viremia On Monotherapy In Other XXX Trials
- A Twelve-Week, Randomized, Double-Blind, Placebo-Controlled, Fixed-Dose, Parallel Group, Multicenter, Study Of The Safety And Efficacy Of XXX In Subjects With Irritable Bowel Syndrome
- An Eight-Week, Randomized, Double-Blind, Placebo-Controlled, Dose Ranging Study To Evaluate Efficacy And Safety Of XXX In Subjects With Irritable Bowel Syndrome
- A Twelve-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Ranging, Phase II Study To Assess The Clinical Efficacy Of XXX In Male Subjects With Irritable Bowel Syndrome
- A Twelve-Week, Randomized, Double-Blind, Placebo-Controlled, Study Of XXX In Female Subjects With Alternating (Diarrhea/Constipation) Irritable Bowel Syndrome
- A Double-Blind, Placebo-Controlled, Randomized, Multicenter Study To Investigate The Safety And Efficacy Of 2mg TID Of XXX Over Twelve Weeks In Diarrhea-Predominant Irritable Bowel Syndrome Subjects
- A Randomized, Double-Blind Trial Comparing The Early Profile Of Heartburn Relief Associated With XXX, 20mg Daily Versus XXX 20mg Once Daily In Gastroesophageal Reflux Disease Patients With An Acute Or Documented History Of Erosive Esophagitis
- A Six-Week, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study, To Assess The Efficacy And Safety Of XXX (6mg. BID) And Placebo In Female Patients With Dyspepsia
- A Randomized, Double-Blind, Placebo-Controlled, Multicenter Two-Week Pilot Study To Evaluate The Efficacy, Safety And Tolerability Of XXX (25 and 100mg. BID) Given Orally In Female Patients With Irritable Bowel Syndrome With Diarrhea (IBS-D)
- A Multicenter, Double-Blind, Placebo-Controlled Efficacy And Safety Study Of Low-Dose XXX In Male Patients With Irritable Bowel Syndrome
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