CompletedPhase 3

Opioid-free Vs Traditional Balanced Anesthesia in Laparoscopic Colorectal Surgery

Spain120 participantsStarted 2022-05-15

Plain-language summary

The goal of this clinical trial is to compare opioid free anesthesia versus opioid anesthesia in patients undergo laparoscopic colorectal surgery. The main question it aims to answer is assess the efficacy of opioid-free anaesthesia respect to postoperative pain control in patients undergoing a laparoscopic colorectal surgery. Participants will answer a questionnaire during the first 3 days of admission, assessing pain through the visual analog scale (VAS). The researchers will compare the consumption of opiates during the postoperative period in the opioid-free anesthesia group.

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: ( - ) Patients older than or equal to 18 years. (-) Patients scheduled for laparoscopic colorectal surgery. (-) Patients with physical status classification (ASA) I-III. (- ) Patients who have signed the informed consent of the clinical trial Exclusion Criteria: (-) Pregnant or lactating patients. (-)Patients with allergy to any of the drugs or excipients used in the study (-) Emergency laparoscopic colorectal surgery (-) Patients with AV block, intraventricular block, or sinus block (-) Adam-Stokes syndrome. (-) Patient on chronic beta-blocker treatment with HR \< 50 bpm (-) Patient with ejection fraction \< 40% known (-) Epilepsy. (-) Surgery converted to open surgery (-) Legally disabled patient (-) Patients with physical status classification (ASA) IV.

What they're measuring

Pain control

Timeframe: 3 days

Trial details

NCT IDNCT05887258

SponsorUnai Ortega Mera

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-05-15

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