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Postoperative Pain in Patients Undergoing Scheduled Laparoscopic Intestinal Resection Surgery

Postoperative Pain Assessment in Patients Undergoing Scheduled Laparoscopic Intestinal Resection Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05222789
Acronym
TAP
Enrollment
105
Registered
2022-02-03
Start date
2019-05-01
Completion date
2024-03-20
Last updated
2024-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain, Acute, Postoperative Pain, Chronic

Brief summary

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.

Detailed description

The transverse abdominal plane (TAP) block is a regional anesthesia technique that blocks the afferent nerves of the anterolateral abdominal wall. This observational prospective study aims to evaluate the postoperative analgesic effect in patients undergoing laparoscopic intestinal resection. ASA I-III patients operated on a scheduled basis, between May 1 and September 30, 2019, by laparoscopy for intestinal cancer resection 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.

Interventions

PROCEDURETAP

The transverse abdominal plane (TAP) block is a regional anesthesia technique performed using ultrasound that blocks the afferent nerves of the anterolateral abdominal wall, injecting local anesthetic in the fascial plane between the deep oblique and the transversus abdominis muscles.

Sponsors

Dr. Negrin University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Postoperative acute pain assessed using Visual Analogue Scale, from 0 to 10from the arrival to the postanesthesia care unit to the 4 postoperative hoursassessed using visual analogue scale
Intraoperative analgesic consumptionfrom the anesthesia induction to the end of the surgeryassessed measuring the perioperative analgesics provided during the intraoperative period following routine clinical practice

Secondary

MeasureTime frameDescription
Postoperative chronic pain assessed using Visual Analogue Scale, from 0 to 102 years postoperativelyassessed using visual analogue scale
Side effectsfrom the arrival to the postanesthesia care unit to the hospital discharge (7 days postoperatively)to record the perioperative side effects secondary to the analgesia administered perioperatively

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026