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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04654715
Other study ID # 69HCL20_0673
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 15, 2020
Est. completion date November 20, 2020

Study information

Verified date February 2021
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Prostate cancer is the first cancer amongst men with more than 50000 cases per year in France. Surgical, radiation, frost, or ultrasound induced rectourethral fistula is a rare complication (<1%) of localized prostatic cancer treatment but hard to manage. Different types of treatment exist: conservatory, trans-sphinteric (York-Masson), transanal, perineal, with or without muscle flap interposition. Gracilis flap interposition for rectourethral fistula management is a promising technique but few cases are described and functional results are scarce. The aim of this study is to present surgical and functional outcomes of rectourethral fistulas surgery with gracilis flap interposition after treatment of localized prostate cancer.


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date November 20, 2020
Est. primary completion date November 20, 2020
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria: - Male over 18 years old - Treated for a localized prostatic cancer (Prostatectomy, cryotherapy, HIFU, radiotherapy) - Affected with a treatment induced Rectourethral fistula Exclusion Criteria: - Rectourethral fistula caused by other pelvic diseases (gynecological or digestif cancer, inflammatory bowel disease, other urogenital issues) - Rectourethral fistula treated by cysto-prostatectomy with urinary tract derivation - Patient under guardianship - Non comprehension of written or spoken French

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Gracilis flap interposition for rectouretral fistula management
Gracilis flap interposition is a surgery for rectouretral fistula

Locations

Country Name City State
France Hôpital Lyon Sud Pierre-Bénite

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Urinary continence Urinary Symptom Profile form (from 0 to 39), a higher score indicating a worse outcome. 3 months after surgery
Primary Fecal continence St. Marks form (from 0 to 26), a higher score indicating a worse outcome. 3 months after surgery
Primary Lower extremity functional No validated form exist for surgical consequences after gracilis retrieval. The form used in this study is specific (Difficulty scale for walking, kneeling, crossing the legs ; limitation of movements since the operation (yes/no and which one) (From 0 to 20), a higher score indicating a worse outcome. 3 months after surgery
Primary Surgical scarring The Patient and Observer Scar Assessment Scale (From 7 to 70), a higher score indicating a worse outcome. 3 months after surgery
Primary Global satisfaction of the surgery Patients will give a number to measure their global satisfaction of the surgery (From 1 to 10), a higher score indicating a better outcome. 3 months after surgery