Actively Recruiting
Low Impact Laparoscopic in Colorectal Resection - PAROS2
Led by University Hospital, Bordeaux · Updated on 2025-05-22
148
Participants Needed
3
Research Sites
193 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To improve post-operative recovery, the concept of Low Impact Laparoscopy was developed in colo-rectal surgery with associating low-pressure pneumoperitoneum and microlaparoscopic surgery. A phase III double-blind, prospective, randomized, controlled, multi-centric trial is designed in the aim to assess the impact of low-pressure pneumoperitoneum with microlaparoscopic instruments on post-operative pain at 24 hours without taking opioids. It is compared with low-pressure laparoscopy with classical laparoscopic instruments in patients undergoing colorectal surgeries.
CONDITIONS
Official Title
Low Impact Laparoscopic in Colorectal Resection - PAROS2
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Scheduled colectomy for malignant or benign pathology
- Right colon: ileocecal resection, right colectomy, right colectomy extended to the middle of the transverse
- Left colon: sigmoidectomy, left colectomy
- Rectal resection without stoma for cancer of the upper rectum
- Patient operable by laparoscopy (classic or robot assisted for the Standard group)
- Age 218 years old
- Patient affiliated to a social security system or beneficiary of the same
- Informing the patient and obtaining free, informed and written consent, signed by the patient and his investigator
You will not qualify if you...
- Laparotomy procedure
- Patients with electronic implant (ex : pacemaker)
- Total or Subtotal Colectomy
- Transverse segmental colectomy
- Left angular colectomy
- Proctectomy with stoma or Total Coloproctectomy
- Patient with stoma
- Probable realization of a stoma during the operation
- Procedure associated with colorectal surgery (except appendectomy or liver biopsy)
- Crohn's disease, Hemorrhagic Rectocolitis (UC)
- Sigmoiditis
- EVA before surgery > 3
- BMI 230
- ASA > 3
- History of laparotomy
- Emergency surgery
- Pelvic Sepsis or Preoperative Fistula
- Pregnant woman, likely to be, or breastfeeding
- Persons deprived of their liberty or under measure of judicial protection (curatorship or guardianship) or unable to give their consent
- Inability to undergo medical monitoring of the trial for geographic, social or psychological reasons
AI-Screening
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Trial Site Locations
Total: 3 locations
1
CH de la Côte Basque
Bayonne, France
Actively Recruiting
2
CHU Bordeaux
Bordeaux, France
Actively Recruiting
3
Ch Libourne
Libourne, France
Actively Recruiting
Research Team
C
Christophe LAURENT
CONTACT
B
Benjamin FERNANDEZ
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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