Not Yet RecruitingN/AOther

Multimodal Anesthesia in Robotic Laparoscopic Nephrectomy

Sponsored by Fundacio Puigvert

NCT ID
NCT07558226
Target Enrollment
80 participants
Start Date
2026-05-02
Est. Completion
2027-11-30

About This Study

It is a prospective, randomized, controlled and superiority clinical trial, with the objective of comparing the effectiveness of multimodal anesthesia versus conventional anesthesia in patients undergoing oncological robotic nephrectomy within a short-stay surgery program (SSA). The effect of no specific drug will be evaluated, but rather the anesthetic approach ologies of surgical patients. The clinical trial will be carried out in a third-level university hospital, between the first half of 2026 and the second half of 2027 and, after approval by the corresponding Clinical Research Ethics Committee.

Conditions Studied

AnesthesiaAnesthesia and Procedure Related Time IntervalsNephrectomy / Methods

Interventions

  • Multimodal anesthesia
  • Conventional anesthesia

Eligibility

Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Patients ≥18 years.
* Indication for elective oncological robotic partial or radical nephrectomy.
* ASA classification I-III.
* Candidates for short-stay surgery according to institutional protocol.
* Signed informed consent.

Exclusion Criteria:

* Chronic opioid use. Defined as continuous opioid use during the 3 months prior to surgery
* Uncontrolled chronic pain. Defined as chronic pain not adequately controlled with usual treatment during the 3 months prior to surgery.
* Contraindications to NSAIDs, regional anesthesia, or drugs of the multimodal protocol.
* Advanced renal failure (GFR \<30 ml/min) at the preanesthetic visit.

Study Locations (1)

Fundacio Puigvert
Barcelona, BARCELONA, Spain

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source