Establishment of Fibroid Tissue Bank
Establishment of a Fibroid Tissue Bank
2 other identifiers
observational
43
1 country
1
Brief Summary
The purpose of this study is to collect information and tissue samples from women with uterine fibroids. The samples will be used to study genes, proteins and other substances in order to better understand the disease process and improve fertility and reproductive health. Women who are scheduled to undergo hysterectomy, myomectomy or other surgery due to uterine fibroids or to an unusual variant of fibroid disease, such as HLRCC or benign metastasizing leiomyomatosis, may be eligible for this study. Tissue samples are collected from participants during surgery. The samples are coded and catalogued for research use. Data collected regarding the surgery include the sample location, surgery type, reason for surgery and the primary and secondary diagnoses. Additional data collected about the participant include date of birth, race, ethnicity, weight, height, smoking status, information about menstrual cycles, medications and family history.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jun 2008
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 30, 2008
CompletedFirst Submitted
Initial submission to the registry
July 3, 2008
CompletedFirst Posted
Study publicly available on registry
July 4, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2016
CompletedJune 1, 2018
September 1, 2016
July 3, 2008
May 31, 2018
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Women aged 21-80 with uterine fibroids
- Medically indicated hysterectomy, myomectomy or other surgery for uterine fibroids.
- Samples from patients with unusual variants of fibroid disease (HLRCC, benign metastasizing leiomyomatosis) will be included. These samples may possibly not arise from the uterus proper, as the leiomyoma may have become located elsewhere in the body.
You may not qualify if:
- Inability to give consent or understand the consent forms.
- HIV-infected tissues will be excluded due to concern of equipment contamination.
- Hepatitis-infected tissues will be excluded due to concern of equipment contamination.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, 20892, United States
Related Publications (3)
Marshall LM, Spiegelman D, Barbieri RL, Goldman MB, Manson JE, Colditz GA, Willett WC, Hunter DJ. Variation in the incidence of uterine leiomyoma among premenopausal women by age and race. Obstet Gynecol. 1997 Dec;90(6):967-73. doi: 10.1016/s0029-7844(97)00534-6.
PMID: 9397113BACKGROUNDLepine LA, Hillis SD, Marchbanks PA, Koonin LM, Morrow B, Kieke BA, Wilcox LS. Hysterectomy surveillance--United States, 1980-1993. MMWR CDC Surveill Summ. 1997 Aug 8;46(4):1-15.
PMID: 9259214BACKGROUNDPayson M, Leppert P, Segars J. Epidemiology of myomas. Obstet Gynecol Clin North Am. 2006 Mar;33(1):1-11. doi: 10.1016/j.ogc.2005.12.004.
PMID: 16504803BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Alan H DeCherney, M.D.
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NIH
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 3, 2008
First Posted
July 4, 2008
Study Start
June 30, 2008
Study Completion
September 1, 2016
Last Updated
June 1, 2018
Record last verified: 2016-09-01