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Search / Trial NCT02566746

Contribution of Percutaneous Endoscopic Caecostomie in the Management of Severe Constipation Refractory to Medical Treatment

Launched by NANTES UNIVERSITY HOSPITAL · Oct 1, 2015

Trial Information

Current as of May 03, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patient betwen 18 and 75 years old
  • Chronic constipation defined by the Rome III classification
  • Transit time with pellets made within 24 months preceding the inclusion visit indicating a transit time of at least 120 hours and/or with a Neurogenic bowel dysfunction ≥ 14 for patients with spina bifida and / or spinal cord injuries.
  • Colonoscopy made within the 5 years preceding the inclusion visit indicating the absence of colorectal organic obstacle
  • Anorectal manometry performed within 24 months preceding the inclusion visit performed to substantiate the information on the type of constipation
  • GIQLI score \<121 and Kess Questionnaire score\> 7, despite medical treatment of constipation including taking a laxative (stimulant laxative orally and / or suppository and / or retrograde enema) more than one times per week for at least two months.
  • Affiliation to a social security
  • - Chronic constipation defined by the Rome III classification
  • Transit time with pellets made within 24 months preceding the inclusion visit indicating an increase of at least 120 hours compared to normal
  • Colonoscopy made within the 24 months preceding the inclusion visit indicating the absence of colorectal organic obstacle
  • Anorectal manometry performed in the 24 months preceding the inclusion visit performed to substantiate the information on the type of constipation
  • Score GIQLI love \<121 and Kess Questionnaire score\> 7, despite medical treatment of constipation including taking a laxative (stimulant laxative orally and / or suppository and / or retrograde enema) more than one times per week for at least two months.
  • Affiliation to a social security scheme
  • Informed consent signed
  • Exclusion Criteria:
  • Severe obesity (BMI\> 40)
  • History of surgical resection of colon
  • Hypothyroidism, electrolyte disorders, insulin-dependent diabetes
  • Acute decompensation of depressive syndrome
  • Immunosuppressive therapy
  • Disorders of hemostasis (TP \<70%, APTT\> 1.5, thrombocytopenia \<70,000 / mm3)
  • Pregnant woman (positive serum beta-hCG) or breastfeeding
  • Adults under guardianship, curatorship or under court protection
  • Participation in another research protocol on the treatment of constipation

About Nantes University Hospital

Nantes University Hospital, a leading academic medical institution in France, is dedicated to advancing healthcare through innovative research and clinical trials. As a prominent sponsor of clinical studies, the hospital integrates cutting-edge scientific exploration with patient care, fostering collaborations among multidisciplinary teams of healthcare professionals and researchers. With a strong emphasis on ethical standards and patient safety, Nantes University Hospital aims to contribute to the development of effective therapies and interventions that enhance patient outcomes and overall public health.

Locations

Nantes, , France

Bordeaux, , France

Rennes, , France

Rouen, , France

La Roche Sur Yon, , France

Clermont Ferrand, , France

Ploemeur, , France

Vannes, , France

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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