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NCT04696666
Tolerability and Efficacy of INSTYLAN in Subjects With Moderate to Severe Hemorrhagic Cystitis
NA trial testing INSTYLAN (Sodium Hyaluronate 80mg/50ml) in Hemorrhagic Cystitis in 30 participants. Status unknown.
30 May 2021
Quick facts
| Lead sponsor | LIDDE Therapeutics |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 15 May 2020 |
| Primary completion | 30 May 2021 |
| Estimated completion | 30 July 2021 |
| Sites | 10 locations across France |
Drugs / interventions tested
- INSTYLAN (Sodium Hyaluronate 80mg/50ml)
Conditions studied
- Hemorrhagic Cystitis — all drugs for Hemorrhagic Cystitis →
Sponsor
LIDDE Therapeutics
Who can join
Adults 18 to 80, any sex, with Hemorrhagic Cystitis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to assess the efficacy and tolerability of INSTYLAN (Sodium Hyaluronate 80mg/50ml) in Patients with early or late symptoms of moderate to severe hemorrhagic cystitis caused by pelvic radiation therapy and/or chemotherapy. The study is conducted in the field of routine clinical practice and will recruit 30 subjects treated with intravesical instillations with INSTYLAN weekly for 6 weeks.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04696666
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Hemorrhagic Cystitis
Currently open trials in the same condition.
- NCT06241274 — Moxibustion in the Treatment of Hemorrhagic Cystitis After Allo-HSCT · NA · recruiting
- NCT06198517 — Moxibustion for the Prevention of Hemorrhagic Cystitis After Allo-HSCT · NA · 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 NCT04696666 (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 LIDDE Therapeutics
- Last refreshed: 6 January 2021
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/NCT04696666.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing