CASPeR: Causes of Low Digestive Bleeding in Proctology

Sponsor
Groupe Hospitalier Paris Saint Joseph (Other)
Overall Status
Completed
CT.gov ID
NCT02846285
Collaborator
(none)
500
1
10
50.2

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Detailed 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.

Study Design

Study Type:
Observational
Actual Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Causes of Low Digestive Bleeding in Proctology
Study Start Date :
Sep 1, 2013
Actual Primary Completion Date :
Jul 1, 2014
Actual Study Completion Date :
Jul 1, 2014

Outcome Measures

Primary Outcome Measures

  1. Assessment of causes and determine the origin of down gastrointestinal bleedings [Within 4 months after surgery]

    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

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All patients with proctological context
Exclusion Criteria:
  • Patients refusing to participate

Contacts and Locations

Locations

Site City State Country Postal Code
1 Groupe Hospitalier Paris Saint Joseph Paris Ile-de-France France 75014

Sponsors and Collaborators

  • Groupe Hospitalier Paris Saint Joseph

Investigators

  • Principal Investigator: FATHALLA Nadia, MD, Groupe Hospitalier Paris Saint Joseph

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Groupe Hospitalier Paris Saint Joseph
ClinicalTrials.gov Identifier:
NCT02846285
Other Study ID Numbers:
  • CASPeR
First Posted:
Jul 27, 2016
Last Update Posted:
Jul 27, 2016
Last Verified:
Jul 1, 2016
Keywords provided by Groupe Hospitalier Paris Saint Joseph
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 27, 2016