CClinicalTrials.gg
Status unknownNCT02919852prolapseUpdated Sep 30, 2016

Laparoscopic Retrovesical Colpopectinopexia

An interventional study of laparoscopic retrovesical colpopectinopexia in Pelvic Organ Prolapse, sponsored by Orel Regional Hospital, Russia. Status unknown at 1 site in Ukraine. Open to female participants. Per ClinicalTrials.gov, last updated 2016-09-30.

Sponsored by Orel Regional Hospital, Russia · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2016), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Not applicable
Sex
Female
01

Study summary

The purpose of this study is to identify whether a new operative technic would be acceptable in female with pelvic organ prolapse.

Read the detailed description

A new operative technic use to treat pelvic organ prolapse in women. Investigators plan to evaluate the results of procedure in the field of recurrence rate, effectiveness, mortality,morbidity and learning curves.

02

Conditions studied

  • Pelvic Organ Prolapse
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In context

Prolapse

676 studies on the registry are indexed under Prolapse; 79 are open to participants now.

This study's planned enrollment of 70 is close to the median of 74 across 435 interventional studies indexed under Prolapse.

Browse Prolapse studies →

Lead sponsor

This is the only study on the registry with Orel Regional Hospital, Russia as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • all female with cystocele 1-2-3 grade? hysterocele 1-2 (POP-Q)

Exclusion criteria

Exclusion Criteria:

  • rectocele more then 1 grade (POP-Q) hysterocele more then 2
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
70 participants (estimated)

Study arms

  • Other
    laparoscopic retrovesical colpopectinopexia

    new operative technic

    Procedure: laparoscopic retrovesical colpopectinopexia

Interventions

  • Procedurelaparoscopic retrovesical colpopectinopexia

    Laparoscopic correction of pelvic organ prolapse using a mesh in retrovesical space with pectineal ligament fixation.

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What researchers measure

Primary outcomes

  1. POP-Q assessment

    assessment of vaginal wall accordion to POP-Q score

    Time frame: first post operation day

Secondary outcomes

  1. POP-Q assessment

    assessment of vaginal wall accordion to POP-Q score

    Time frame: 6 month after operation

  2. POP-Q assessment

    assessment of vaginal wall accordion to POP-Q score

    Time frame: 1 year after operation

07

Study locations

1 of 1 sites recruiting
  • LISOD
    Kiev, Ukraine
    • Sergey Baydo, MD, PhD · Contact · surgyserg@gmail.com · +380504415892
    • Bekhan Khatsiev, MD,PhD · Sub investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 30, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02919852
Lead sponsor
Orel Regional Hospital, Russia
Responsible party
Sponsor
First posted
Sep 29, 2016
Start date
Sep 2016
Primary completion
Sep 2018 (estimated)
Completion
Jun 2019 (estimated)
Last update
Sep 30, 2016

Study contacts

Alexey Abolmasov, MD,PhD
Contact
abolmasov57@gmail.com
+79107478534

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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