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Clinical trialNCT00459134CompletedInterventional

L-Arginine Supplements in Treating Women Who Are Cancer Survivors

SponsorWake Forest University Health SciencesEnrollment186Sexual DysfunctionSexuality and Reproductive IssuesUnspecified Adult Solid Tumor, Protocol Specific
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

25 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Ccop - Christiana Care Health Services

    Newark, Delaware, United States

  • Ccop - Mount Sinai Medical Center

    Miami Beach, Florida, United States

  • Mbccop - Medical College of Georgia Cancer Center

    Augusta, Georgia, United States

  • Mbccop - Jhs Hospital of Cook County

    Chicago, Illinois, United States

  • Ccop - Central Illinois

    Decatur, Illinois, United States

  • Ccop - Northern Indiana Cr Consortium

    South Bend, Indiana, United States

  • Cedar Rapids Oncology Associates

    Cedar Rapids, Iowa, United States

  • Mbccop - Lsu Health Sciences Center

    New Orleans, Louisiana, United States

  • Feist-Weiller Cancer Center at Louisiana State University Health Sciences

    Shreveport, Louisiana, United States

  • Ccop - Michigan Cancer Research Consortium

    Ann Arbor, Michigan, United States

  • Ccop - Beaumont

    Royal Oak, Michigan, United States

  • Ccop - Cancer Research for the Ozarks

    Springfield, Missouri, United States

  • Ccop - Heartland Research Consortium

    St Louis, Missouri, United States

  • Ccop - St. Louis-Cape Girardeau

    St Louis, Missouri, United States

  • Hematology Oncology Associates of Central New York, Pc - Northeast Center

    East Syracuse, New York, United States

  • Ccop - North Shore University Hospital

    Manhasset, New York, United States

  • Alamance Cancer Center at Alamance Regional Medical Center

    Burlington, North Carolina, United States

  • Hugh Chatham Memorial Hospital

    Elkin, North Carolina, United States

  • Southeastern Medical Oncology Center - Goldsboro

    Goldsboro, North Carolina, United States

  • Caldwell Memorial Hospital

    Lenoir, North Carolina, United States

  • Wake Forest University Comprehensive Cancer Center

    Winston-Salem, North Carolina, United States

  • Ccop - Columbus

    Columbus, Ohio, United States

  • Ccop - Main Line Health

    Wynnewood, Pennsylvania, United States

  • Ccop - Upstate Carolina

    Spartanburg, South Carolina, United States

  • Ccop - Sioux Community Cancer Consortium

    Sioux Falls, South Dakota, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
1 May 2007
Primary completion
1 Jun 2010
Completion
1 Jun 2010
Last update posted
28 Sept 2021
Registered enrollment
186
Registry id
NCT00459134

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.