Last updated: September 14, 2023
Sponsor: West China Hospital
Overall Status: Active - Not Recruiting
Phase
2/3
Condition
Gynecological Infections
Urinary Incontinence
Urinary Tract Infections
Treatment
Interferon
Sodium Hyaluronate
Sodium Chloride Injection
Clinical Study ID
NCT05912946
2022370
Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients over 18 years old, regardless of gender
- Combined with bladder pain/discomfort during urination, and at least one lower urinarytract symptom such as frequency and urgency, duration > 6 months
- The total score of O'Leary-Sant ICSI+ICPI is more than 18 points
- Agree to receive bladder perfusion therapy
Exclusion
Exclusion Criteria:
- Have a history of allergy to interferon drugs
- Patients with serious heart, lung, liver, kidney or blood diseases, abnormal liverfunction, renal insufficiency, etc.
- Pregnant or lactating women
- A history of urinary tract infection within 12 weeks
- IC/ BPS-like symptoms caused by urinary diseases, such as overactive bladder,neurogenic bladder, urinary calculi, radiation cystitis, and endometriosis
- Within 24 weeks, patients had the following treatment history: bladder hydrodilation,intravesical laser treatment, pelvic floor reconstruction surgery
- Patients who have taken related drugs or participated in other clinical studies andreceived study drugs or medical device interventions within 3 months
Study Design
Total Participants: 129
Treatment Group(s): 3
Primary Treatment: Interferon
Phase: 2/3
Study Start date:
October 15, 2023
Estimated Completion Date:
October 15, 2024