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Platelet Enriched Plasma for Treatment of Interstitial Cystitis

M

Mansoura University

Status and phase

Unknown
Phase 2
Phase 1

Conditions

Interstitial Cystitis
Platelet Enriched Plasma
Bladder Pain Syndrome

Treatments

Biological: platelet enriched plasma

Study type

Interventional

Funder types

Other

Identifiers

NCT04118946
MS.19.03.540

Details and patient eligibility

About

A prospective randomized trial will be conducted aiming at evaluation the efficacy and safety of platelet enriched plasma for management of bladder pain syndrome .

Enrollment

33 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with a diagnosis of interstitial cystitis/ Bladder painful Syndrome for more than 3 months will be enrolled

Exclusion criteria

  • Patients with Anemia, blood disorders, history of pelvic irradiation, pelvic malignancy, and active urinary tract infection unless treated, vesical stone, gynecological disorders e.g. uterine fibroid and neurological disorders will be excluded. Patients less than 18 years old will not be allowed to participate.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

33 participants in 2 patient groups

intravesical instillation
Active Comparator group
Description:
Intravesical instillation of platelet enriched plasma every week for 6 weeks
Treatment:
Biological: platelet enriched plasma
submucosal injection
Active Comparator group
Description:
submucosal injectionof platelet enriched plasma
Treatment:
Biological: platelet enriched plasma

Trial contacts and locations

1

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Central trial contact

Mohamed Attia; Ahmed S El Hefnawy, MD

Data sourced from clinicaltrials.gov

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