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Clinical Trials/DRKS00021072
DRKS00021072
Completed
Not Applicable

Retrospective monocentric cohort study to evaluate the efficacy and safety of Splentis for transvaginal sacrospinal fixation of the primary apical prolapse - Rexo

Promedon GmbH0 sites110 target enrollmentMarch 16, 2021
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ConditionsN81.4Uterovaginal prolapse, unspecified

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
N81.4
Sponsor
Promedon GmbH
Enrollment
110
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 16, 2021
End Date
September 30, 2020
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. women \= 18 Jahre
  • •2\. History of transvaginal bilateral sacrospinal fixation by splentis of an apical pelvic organ prolapse
  • •3\. Signed informed consent

Exclusion Criteria

  • •1\. Patient is unwilling or capable of giving informed consent

Outcomes

Primary Outcomes

Not specified

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