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Effect of platelets Rich Plasma in recurrent cystitis in women

Effect of platelets Rich Plasma in recurrent cystitis in women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017092336363N1
Enrollment
30
Registered
2017-11-11
Start date
2016-09-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

recurrent cystitis. cystitis

Interventions

Intervention 1: platelet rich plasma 20cc intra bladder instillation second time 2 weeks after first time and third and fourth times 1 month after previous time. Intervention 2: normal salin 20cc intr
Treatment - Drugs
Placebo
platelet rich plasma 20cc intra bladder instillation second time 2 weeks after first time and third and fourth times 1 month after previous time
normal salin 20cc intra bladder instillation second time 2 weeks after first time and third and fourth times 1 month after previous time

Sponsors

vice chancellor for research,kerman of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: inclusionn criteria: women aged more than 18 years ; who refere to urology clinic due to recurrent cystitis exclusion criteria: any congenital urologic anomalies ; vesicoureteral reflux ; ureteral duplicasion ; ureterocele ; ureteral diverticulom ; history of other urologic diseases ; interstitial cystitis ; urinary stone ; carcinum insitue of bladder ; history of nurologic disease ; IUD or spermcidal agent usage

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Urinary infection. Timepoint: during the intervention and 2 month and 12 month after intervention. Method of measurement: urinary culture.;Irritative urinary symptoms. Timepoint: during and 2 months and 12 months after intervention. Method of measurement: ICIQ-OAB questionnare.

Secondary

MeasureTime frame
Age. Timepoint: during of intervention. Method of measurement: questionnare.;Weight. Timepoint: during of intervention. Method of measurement: questionnare.;Marriage. Timepoint: during of intervention. Method of measurement: questionnare.;Education. Timepoint: during of intervention. Method of measurement: questionnare.;Number of delivery. Timepoint: during of intervention. Method of measurement: questionnare.;Smoking. Timepoint: during of intervention. Method of measurement: questionnare.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmahbube mirzaei

kerman medicine universiry

mirzaeimahboubeh@yahoo.com+98 34 3222 1600

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026