Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Outcome Measure:

pain/discomfort of endometrial biopsy

Outcome Time Frame:

during procedure

Principal Investigator

Joan MG Crane, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Faculty, Discipline Obstetrics and Gynecology, Memorial University of Newfoundland

Authority:

Canada: Health Canada

Study ID:

HIC02.159

NCT ID:

NCT00200226

Start Date:

February 2003

Completion Date:

September 2007

Related Keywords:

• Endometrial Biopsy
• pain/discomfort
• cervical dilatation
• side effects
• Adenoma