Viewing Study NCT03195361


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Study NCT ID: NCT03195361
Status: COMPLETED
Last Update Posted: 2021-02-03
First Post: 2016-05-01
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Multicenter, Prospective, Non-randomized, Single-arm, Interventional Study for the Evaluation of the Safety and Preformance of the SRS Device for the Treatment of Pelvic Organ Prolapse
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Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
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Bio Spec Retention: None
Bio Spec Description: None
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Phases

Phase Brief Phase Text View
None NA View
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