Postoperative Pain in Patients Undergoing Scheduled Laparoscopic Intestinal Resection Surgery
CompletedNCT05222789
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
This observational prospective study aims to evaluate the postoperative analgesic effect of a regional anesthesia thechnique (TAP block) in patients undergoing scheduled laparoscopic intestinal resection for intestinal cancer. ASA I-III patients operated between May 1 and September 30, 2019 under general anesthesia according to usual clinical practice, will be included. Patients who meet any of the following criteria will be excluded from this study: under 18 years old, language barrier, cognitive impairment or inability to assist in clinical assessment, drug or alcohol abuse, intake of opioids, consumption of analgesics 24 hours before surgery, BMI \<18 or \>35 kg/m2. Subsequently, an analysis will be made evaluating the quality of analgesia and the appearance of postoperative chronic pain and comparing the patients who underwent TAP block with those who did not.
Study details
- Official title
- Postoperative Pain Assessment in Patients Undergoing Scheduled Laparoscopic Intestinal Resection Surgery
- Interventions
- Procedure: TAP
- Sponsor
- Hospital Universitario de Gran Canaria Doctor Negrín
- Start date
- 2019-05-01
- Primary completion
- 2024-03-20
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- Spain
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * ASA I-III * Operated on a scheduled basis for laparoscopic intestinal cancer resection Exclusion Criteria: * Under 18 years old * Language barrier * Cognitive impairment or inability to collaborate in clinical assessment during the study * Drug or alcohol abuse * Habitual intake of opioids * Consumption of analgesics 24 hours before surgery * BMI \<18 or \>35 kg/m2
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05222789