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NCT03301818
Vaginal Elasticity Assessment Before and After Surgical Repair for Urinary Stress Incontinence.
NA trial testing Vaginal tactile imager in Stress Incontinence, Female in 23 participants. Completed in 20 July 2020.
30 June 2020
Quick facts
| Lead sponsor | Rambam Health Care Campus |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | diagnostic |
| Enrollment | 23 |
| Start date | 1 August 2018 |
| Primary completion | 30 June 2020 |
| Estimated completion | 20 July 2020 |
| Sites | 1 location across Israel |
Drugs / interventions tested
- Vaginal tactile imager
Conditions studied
- Stress Incontinence, Female — all drugs for Stress Incontinence, Female →
Sponsor
Rambam Health Care Campus — full company profile →
Who can join
Adults 18 to 75, female only, with Stress Incontinence, Female. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Female patients with USI will be evaluated for vaginal elasticity using vaginal tactile imaging both before and after surgery for the repair of the USI. Surgical repair will be performed by a single surgeon who will perform a tension free vaginal tape obturator (TVT-O) repair.
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 NCT03301818
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Vaginal tactile imager
Trials testing the same drug.
- NCT04114019 — The Effect of Pelvic Floor Physiotherapy on Vaginal Elasticity · withdrawn
- NCT03930290 — Physiologic Elasticity Changes During Pregnancy and After Labor. · terminated
Other recruiting trials for Stress Incontinence, Female
Currently open trials in the same condition.
- NCT06885463 — PRP & PDO Threads in Treatment of Stress Incontinence · NA · recruiting
Other Rambam Health Care Campus trials
Trials by the same sponsor.
- NCT07384013 — Study Protocol: Impact of Metamizole (Optalgin®) on Anti-Xa Concentrations in Oncology Patients Receiving DOACs · NA · recruiting
- NCT06688253 — Intravenous Human IgG1 Fc Fragment (Efgartigimod) in Myasthenic Crisis · Phase 4 · not yet recruiting
- NCT06235749 — Administration Of Calcium Gluconate for The Reduction of Blood Loss During Elective Cesarean Delivery · NA · recruiting
- NCT06622902 — Influence of Flow Rate Change on CO2 Levels During High Flow Nasal Ventilation (HFNV) in Preterm Infants. · NA · recruiting
- NCT05922111 — Cervical Ripening Balloon for 12 Hours vs. 1 Hour. · NA · not yet recruiting
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 NCT03301818 (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 Rambam Health Care Campus
- Last refreshed: 27 July 2020
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/NCT03301818.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing