Ireland
--:--IST
Recruiting Observational

Incisional heRnia dIgestion Sexuality

NCT05596357 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2023-07-10
Last updated
2023-09-08

Condition(s) studied

Incisional Hernia

Investigational drug(s) / intervention(s)

questionnaires

questionnaires: The patient must answer questionnaires before and after reconstructive surgery

Study summary

After an operation on the abdomen, some patients present with an incisional hernia(incisional hernia) which causes a permanent exteriorization of the vicera. This situation is at the origin of postural problems. Surgery which consists both of reducing pain and correcting the functional limitation and aesthetic damage helps restore normal anatomy and improve muscle tension of the wall, restore the musculoskeletal balance of the trunk and thus the cardio-respiratory and motor functions of patients. The resulting benefits on quality of life and reduction of chronic pain have been demonstrated by several studies. This study tends to better understand the functional and sexual prejudices linked to these parietal pathologies by passing questionnaires to the operated patients

Eligibility

Sex
ALL
Min age
18 Years
Max age
79 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged 18 to 79 * No opposition to research * Planned surgery to cure a hernia or complex anterior eventration of the abdomen by laparotomy or laparoscopy * Mastery of the French language sufficient to answer questionnaires * Registration in a national health care system Exclusion Criteria: * Emergency surgery * ASA (American Society of Anesthesiologists) score\> 3 during the preoperative consultation * Current pregnancy or breastfeeding * Patient under guardianship or curatorship * Patient under AME (State Medical Aid)

Primary outcome measure(s)

  • Symtoms of constipation --> Patient Assessment of Constipation Symptoms (PAC-SYM) — 25 months
    Analyze changes in symptoms related to constipation before (1 month) and after surgical operation (M3, M12 and M24)

Trial sites (1)

FacilityCityRegionStatus
David Moszkowicz Colombes Île-de-France Region Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05596357 on ClinicalTrials.gov ↗ ← All trials in France