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NCT03809806
Four-arm Mesh for Vaginal Stump Prolapse
NA trial testing 4-arm polypropylene mesh surgery in Pelvic Organ Prolapse in 180 participants. Completed in 31 December 2017.
31 December 2017
Quick facts
| Lead sponsor | Medical University of Lublin |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 180 |
| Start date | 1 January 2014 |
| Primary completion | 31 December 2017 |
| Estimated completion | 31 December 2017 |
| Sites | 1 location across Poland |
Drugs / interventions tested
- 4-arm polypropylene mesh surgery
- The Female Sexual Function Index (FSFI) questionnaire
- King Health Questionnaire (KHQ)
- Pelvic Organ Prolapse Quantification (POPQ) staging
- Postoperative questionnaire
- The Short Form Health Survey (SF 36) questionnaire
Conditions studied
- Pelvic Organ Prolapse — all drugs for Pelvic Organ Prolapse →
- Sexual Function Abnormal — all drugs for Sexual Function Abnormal →
Sponsor
Medical University of Lublin
Who can join
Adults 18 to 75, female only, with Pelvic Organ Prolapse or Sexual Function Abnormal. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
To estimate the safety and efficacy of performing modified anterior transvaginal mesh surgery using polypropylene mesh for treatment of advanced urogenital prolapse after hysterectomy (stage III and IV vc Pelvic Organ Prolapse Quantification \[POP-Q\] system staging).
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03809806
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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Other Medical University of Lublin trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03809806 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Medical University of Lublin
- Last refreshed: 18 January 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03809806.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing