Skip to content

Subjective and objective outcome after laparoscopic sacrocolpopexy

Subjective and objective outcome after laparoscopic sacrocolpopexy - SOOS-study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42649
Enrollment
189
Registered
2016-02-09
Start date
2015-01-01
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

(recidief) prolaps recurrent vaginal prolapse vaginal vault prolapse

Interventions

None listed

Sponsors

Diakonessenhuis Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Patients who underwent a laparoscopic sacrocolpopexy in the period from August 2004 to December 2014 in Diakonessenhuis Utrecht/Zeist - With good understanding of the Dutch language and willing to complete the validated questionnaire - Willing to participate in a outpatient clinic visit to undergo a gynaecological examination.

Exclusion criteria

Exclusion criteria: A potential subject who meets not any of the above mentioned inclusion criteria will be excluded from participation in this study: insufficient understanding of Dutch language and not willing to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Subjective effectiveness of the laparoscopic sacrocolpopexy: by evaluating the validated questionnaire filled in by the eligible patients.

Secondary

MeasureTime frame
- objective effectiveness bij gynaecological examination - safety of the procedure by evaluating the per- and postoperative complications. - evaluating the actual quality of life, remaining or new urogynaecologic symptoms and signs 1-11 years postsurgery by a validated questionnaire.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)