Last reviewed · How we verify

NCT04696666

Tolerability and Efficacy of INSTYLAN in Subjects With Moderate to Severe Hemorrhagic Cystitis

Status unknown NA Last updated 6 January 2021
What this trial tests

NA trial testing INSTYLAN (Sodium Hyaluronate 80mg/50ml) in Hemorrhagic Cystitis in 30 participants. Status unknown.

Timeline
15 May 2020
Primary endpoint
30 May 2021
30 July 2021

Quick facts

Lead sponsorLIDDE Therapeutics
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date15 May 2020
Primary completion30 May 2021
Estimated completion30 July 2021
Sites10 locations across France

Drugs / interventions tested

Conditions studied

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.

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Other recruiting trials for Hemorrhagic Cystitis

Currently open trials in the same condition.

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Data sources for this page

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