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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02846285
Other study ID # CASPeR
Secondary ID
Status Completed
Phase N/A
First received July 21, 2016
Last updated July 22, 2016
Start date September 2013
Est. completion date July 2014

Study information

Verified date July 2016
Source Groupe Hospitalier Paris Saint Joseph
Contact n/a
Is FDA regulated No
Health authority France: Ministry of HealthFrance: Committee for the protection of Persons
Study type Observational

Clinical Trial Summary

The various causes of bleeding Proctological are well known to gastroenterologists in clinical practice but their proportions have not, to our knowledge, been dedicated epidemiological studies. Investigators wanted to evaluate this data as part of a specialized consultation. Investigators have prospectively collected the causes of gastrointestinal bleeding down the patients seen two of us in specialized proctology center. A clinical examination including an inspection, palpation and feel, and a anoscopy (when possible) were made during the consultation. Local levies referred (s) histological and / or infection were also carried out if necessary. When she had not been made, a colonic exploration was offered to all patients over 45 years and / or when indicated by the pathological context. When there were several possible causes, the clinician holding one that seemed to be the main. Patients consulting within four months postoperatively a proctology action were not included. The study period extended from September 2013 to July 2014 inclusive. The collection of anonymous data.


Description:

The various causes of bleeding Proctological are well known to gastroenterologists in clinical practice but their proportions have not, to our knowledge, been dedicated epidemiological studies. Investigators wanted to evaluate this data as part of a specialized consultation. Investigators have prospectively collected the causes of gastrointestinal bleeding down the patients seen two of us in specialized proctology center. A clinical examination including an inspection, palpation and feel, and a anoscopy (when possible) were made during the consultation. Local levies referred (s) histological and / or infection were also carried out if necessary. When she had not been made, a colonic exploration was offered to all patients over 45 years and / or when indicated by the pathological context. When there were several possible causes, the clinician holding one that seemed to be the main. Patients consulting within four months postoperatively a proctology action were not included. The study period extended from September 2013 to July 2014 inclusive. The collection of anonymous data.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date July 2014
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender Both
Age group 45 Years and older
Eligibility Inclusion Criteria:

- All patients with proctological context

Exclusion Criteria:

- Patients refusing to participate

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Other:
No intervention


Locations

Country Name City State
France Groupe Hospitalier Paris Saint Joseph Paris Ile-de-France

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of causes and determine the origin of down gastrointestinal bleedings Determine the origine of gastrointestinal bleedings from the below:
Internal hemorrhoidal pathology
Anal Fissure
Perianal Crohn lesions
Cryto-glandular Anal fistula
Thrombosis external hemorrhoidal
Anal condylomata and / or perianal
Syndrome solitary rectal ulcer without prolapse externalized
Ano-radiation proctitis
Anal dermatitis and / or perianal
Complete Rectal prolapse externalized
Ulcerative colitis Recto
other
Within 4 months after surgery No
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