Dr. Eid's Research and Grants on Penile Implants

Research Activities / Industrial Grants

  • A Multicenter, Randomized, Parallel Group, Double-Blind, Placebo Controlled, Flexible Dose Escalation Study to Evaluate Self-Esteem and Overall Relationships in Men with Erectile Dysfunction Treated with Viagra (Sildenafil Citrate) in the United States.
    Pfizer - Investigator Meeting: April 2001

  • A Randomized, Double-Blind, Placebo Controlled Study of the Efficacy and Safety of IC351(LY450190) Administered “On Demand” to Patients with Erectile Dysfunction.
    Lily-ICOS  - Starting Date: 2000

  • A Randomized, Double-Blind Study (With Open Label Treatment Extension) to Evaluate the Efficacy and Safety of Viagra (Sildenafil) in Men with Symptoms of Depression and Erectile Dysfunction.
    Pfizer - Starting Date: September 1997

  • An Open, Non-Comparative Extension Study of Sildenafil in Patients with Erectile Dysfunction
    Pfizer - Starting Date: August 1977

  • An Open, Non-Comparative Study to Assess the Long-Term Safety of Sildenafil in Patients with Erectile Dysfunction.
    Pfizer - Starting Date: August 1996

  • Multi-Center Prospective cohort Study to Evaluate the Safety and Effectiveness of The American Medical Systems (AMS) Ambicor Inflatable Penile Prosthesis. American Medical Systems, Inc.
    Pfizer Hospital Products Group - Starting Date: 1996

  • A Double-Blind, Randomized, Placebo-Controlled Parallel Group, Fixed-Dose, Multi-Center Study to Assess the Efficacy and Safety of UK-92, 480, Administered Over Six Months to Male Patients with Erectile Dysfunction.
    Pfizer - Starting Date: February 1996

  • Long-Term Evaluation of the Safety and Efficacy of Alprostadil Administered by MUSE.
    Vivus - Starting Date: 1995

  • A Placebo-Controlled Safety and Efficacy Study of Alprostadil Alphadex (PGE 1-Cyclodetrin) in the Treatment of Erectile Dysfunction in Diabetic and Non-Diabetic Patients Followed by 48 Weeks of Open Label Treatment.
    Schwarz Pharma - Starting Date: October 1993

  • Treatment of Erectile Failure with Medicated Urethral System for Erection (MUSE).
    Vivus - June 1993 to Present

  • Pilot Study with Alprostadil Sterile Powder (PGE 1) in Erectile Dysfunction. Protocol M/56FP50/0074
    Upjohn - 1992 to May 1993

  • No Effect & Lowest Effective Dose-Finding Study of Alprostdil Sterile Powder (PGE1 in Erectile Dysfunction. Protocol M/56FP50/0080
    Upjohn - January 1993 to April 1993.

  • Long-Term Safety Study of Alprostdil Sterile Powder (PGE 1 Alprostadile Sterile Powder in Patients with Erectile Dysfunction. Protocol M/5650/0070
    Upjohn - Starting Date November 1992- present


J. Francois Eid, MD, receives or has received research support/grants from Coloplast Corporation, American Medical Systems (AMS), Lilly ICOS LLC Bayer, Vivus, Pharmacia-Upjohn and Pfizer Inc. He is/was a consultant and on the speakers bureau for Coloplast, AMS, Lilly ICOS LLC, Bayer and Pfizer Inc.