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Spots Global Cancer Trial Database for A Multicenter Prospective Non-Interventional Study Assessing the Management of Canadian Women With Uterine Fibroids

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Trial Identification

Brief Title: A Multicenter Prospective Non-Interventional Study Assessing the Management of Canadian Women With Uterine Fibroids

Official Title: A Multicentre Prospective Non-interventional Study Assessing the Management of Canadian Women With Uterine Fibroids, a Patient Registry

Study ID: NCT02580578

Conditions

Leiomyoma

Interventions

No Intervention

Study Description

Brief Summary: This study will characterize the treatments and outcomes associated with different uterine fibroid treatments in Canada, to understand patients' preferences and satisfaction with different medical and procedural interventions. The study will also assess the effectiveness of ulipristal acetate (Fibristal®) in controlling bleeding, reducing fibroid volume and symptoms, and improvement in patient's quality of life.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Peter Lougheed Centre/University of Calgary, Calgary, Alberta, Canada

Urestky Edmonton Clinic, Edmonton, Alberta, Canada

Sanders Vancouver Clinic, Vancouver, British Columbia, Canada

Children's and Women's Health Centre of British Columbia - The University of British Columbia, Vancouver, British Columbia, Canada

Southern Health Centre, White Rock, British Columbia, Canada

Landau Fredericton Clinic, Fredericton, New Brunswick, Canada

Strand Clinic, St. John, Newfoundland and Labrador, Canada

IWK Healtch Centre, Halifax, Nova Scotia, Canada

Hamilton Health Sciences, Hamilton, Ontario, Canada

Minimally Invasive Gynecology Clinic, London, Ontario, Canada

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada

St. Micheals Hospital, Toronto, Ontario, Canada

Mount Sinai Hospital, Toronto, Ontario, Canada

South Windsor Women's Health, Windsor, Ontario, Canada

Centre Gynécologie et Maternité, Lasalle, Quebec, Canada

Jewish General Hospital, Montreal, Quebec, Canada

Clinique de Gynécologie & Obstétrique Pierre Boucher, Montreal, Quebec, Canada

Complexe Medical Saint-Laurent, Saint-Laurent, Quebec, Canada

University of Saskatchewan, Regina, Saskatchewan, Canada

CHU de Québec-Universite Laval, Québec, , Canada

Contact Details

Name: Carmen Enciu

Affiliation: Allergan

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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