Randomized Study in the Prevention of Pain Shoulders After Laparoscopic Surgery (NCT06039761) | Clinical Trial Compass
CompletedNot Applicable
Randomized Study in the Prevention of Pain Shoulders After Laparoscopic Surgery
France190 participantsStarted 2023-12-13
Plain-language summary
The purpose of this study is to assess shoulder pain at rest (average over the last 24 hours) assessed by visual analogue scale from 0 to 100mm on Day 1.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age ≥ 18 years;
* Celiosurgery including a Transversus Abdominis Plane block with multimodal analgesia;
* Planned laparoscopic surgery for gallbladder, inguinal hernia, umbilical hernia, incisional hernia repair, adnexectomy, oophorectomy, endometriosis, tube ligation;
* Affiliation to the social security scheme;
* Signed informed consent
Exclusion Criteria:
* Celiosurgery such as colectomy, bariatric surgery, hysterectomy, prostatectomy, nephrectomy;
* Surgical emergency;
* History of chronic obstructive pulmonary disease;
* Weight less than 50 kg;
* Consumption of preoperative opioids;
* Antidepressant treatment and/or anxiolytic treatment;
* Conversion by laparotomy;
* Intraperitoneal sepsis;
* Major intraoperative complication (hemorrhage, anaphylaxis, etc.);
* Other surgical or medical interventions planned during the study;
* Patient participating in another clinical trial, or during a period of exclusion from another clinical trial;
* Inability to understand information related to the study;
* Woman who is pregnant or likely to be pregnant (of childbearing age, without effective contraception) or currently breastfeeding;
* Patient deprived of liberty or under guardianship or curatorship or unable to give consent.
What they're measuring
1
Shoulder pain at rest assessed by visual analog scale