Last updated: 11/07/2018 13:22:53
A combined report for protocols SB223030/015 and SB223030/016: a randomized, double-blind, placebo-controlled trial of the effect of idoxifene in the prevention of bone loss in early postmenopausal women and a randomized, double-blind, placebo-controlled trial of the effect of idoxifene in the p ...
Clinicaltrials.gov ID
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EudraCT ID
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EU CT Number
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Trial status
Study complete
Study complete
Trial overview
Official title: A combined report for protocols SB223030/015 and SB223030/016: a randomized, double-blind, placebo-controlled trial of the effect of idoxifene in the prevention of bone loss in early postmenopausal women and a randomized, double-blind, placebo-controlled trial of the effect of idoxifene in the p ...
Trial description: A combined report for protocols SB223030/015 and SB223030/016: a randomized, double-blind, placebo-controlled trial of the effect of idoxifene in the prevention of bone loss in early postmenopausal women and a randomized, double-blind, placebo-controlled trial of the effect of idoxifene in the p ...
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
An Assessment of the Value of Ultrasonographic Screening for Endometrial Disease in Postmenopausal Women Without Symptoms. Jan 2001. Fleischer, Arthur C, MD, Wheeler, James, MD, Lindsay, Iain, M.D., Hendrix, Susan, DO, Grabill, Scott, BSc, Kravitz, Barbara, MS, MacDonald, Brian, M.D., Ph.D. American Journal of Obstetrics and Gynecology 184 (2), 70-75
Medical condition
Osteoporosis
Product
idoxifene
Collaborators
Not applicable
Study date(s)
N/A to Invalid Date
Type
Not applicable
Phase
3
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
Not applicable
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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