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Clinical Trials/ACTRN12610000879066
ACTRN12610000879066
Not yet recruiting
未知

Prospective study of single incision transvaginal mesh with single incision polipropilene mesh with transfascial midurethral and apical fixation for treatment of anterior and apical vaginal wall prolapses

Promedon0 sites60 target enrollmentOctober 19, 2010
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Promedon
Enrollment
60
Status
Not yet recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 19, 2010
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Promedon

Eligibility Criteria

Inclusion Criteria

  • •pregnancies defined
  • •no diseases with contraindications for anesthesia
  • •anterior vaginal prolapse with point Ba \> \+1 (POP\-Q classification)

Exclusion Criteria

  • •point Bp \> \-1 or point C \> \-1 (POP\-Q classification),
  • •without tumoral diseases
  • •without urinary infections
  • •without vaginal infections
  • •no previous radioterapy
  • •no pregnancy
  • •no blood dyscrasias or immunosuppression
  • •no psychiatric or neurological diseases

Outcomes

Primary Outcomes

Not specified

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