Condition: Adenocarcinoma (NOS) · Sponsor: Centre Hospitalier Departemental Vendee
Abdomino-perineal resection is a surgical procedure involving the removal of the rectum and anus via abdominal and perineal approaches. During this procedure, a terminal colostomy is created and the perineum is closed. This procedure is indicated for patients with non-metastatic adenocarcinoma of the lower and very lower rectum (where preservation of the sphincter apparatus is not possible) or squamous cell carcinoma of the anal canal that does not respond to chemoradiotherapy. Most often, treatment for non-metastatic adenocarcinoma of the lower and very lower rectum is part of a therapeutic sequence that includes neoadjuvant chemoradiotherapy followed by surgery 7 to 12 weeks later. Recently, the GRECCAR group (Rectal Surgery Research Group) published the results of the Prodigy 23 study demonstrating the benefit of intensification chemotherapy prior to neoadjuvant chemoradiotherapy. This neoadjuvant regimen, and in particular chemoradiotherapy, can lead to impaired postoperative wound healing due to radiation-damaged tissue. The incidence of impaired wound healing following chemoradiotherapy varies in the literature, with rates ranging from 30% to 70%. These wound complications can lead to local skin infections that may progress to pelvic sepsis, resulting in septic shock. The perineum can be closed directly with a skin suture, but perineal reconstructions using a musculocutaneous flap have also been described. These reconstruction techniques require more extensive opera…
This description comes directly from the study's public registry record.
Agnès DORION · 2 51 44 63 80 · agnes.dorion@ght85.fr
Always discuss trial participation with your own doctor first.
| Chu Amiens | Amiens, France | Not Yet Recruiting |
| Chu Angers | Angers, France | Not Yet Recruiting |
| Chd Vendee | La Roche-sur-Yon, France | Recruiting |
| Hospital Saint Antoine (Aphp) | Paris, France | Not Yet Recruiting |
| Chu Rennes | Rennes, France | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT07489820