Clinical trials

3

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Swap Anesthetic Versus Continuous Desflurane in Adults Undergoing Bariatric Surgery

This randomized, parallel-group, non-inferiority clinical trial aims to evaluate whether an anesthetic swap strategy consisting of sevoflurane followed by desflurane 30 minutes before the end of surgery is non-inferior to continuous desflurane anesthesia with respect to extubation time in adults undergoing elective laparoscopic bariatric surgery. Secondary outcomes include time to achieve a Patient State Index (PSi) greater than 80, time to achieve an Aldrete score of at least 8, incidence of postoperative nausea and vomiting, post-anesthesia care unit length of stay, and desflurane-related costs.

Participants needed: 82
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Clínica DávilaUpdated: Aug 5, 2026Locations: 1
Eligibility criteria

Age 18 years or older. [+4]

Surgical procedure lasting less than 2 hours. [+11]

Status: Not yet recruiting

Acceleromyography Versus Electromyography for Neuromuscular Recovery Assessment at the End of Surgery

This prospective observational study aims to evaluate the agreement between acceleromyography and electromyography for measuring train-of-four (TOF) ratio at the end of surgery before reversal of neuromuscular blockade. Adult patients undergoing elective laparoscopic cholecystectomy under general anesthesia with non-depolarizing neuromuscular blockade will undergo simultaneous TOF measurements using both monitoring methods. The study will assess the agreement between the two techniques, estimate measurement bias and limits of agreement, and determine the frequency of clinically relevant disagreement that could affect assessment of neuromuscular recovery and safe extubation.

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Clínica DávilaUpdated: Jul 31, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older. [+3]

Pre-existing neuromuscular disease. [+3]

Status: Recruiting

Analgesia With Transdermal Buprenorphine Patch in Adults Undergoing Video-Assisted Thoracoscopic Surgery

Postoperative pain remains a major challenge after video-assisted thoracoscopic surgery (VATS), despite the use of multimodal analgesia. This randomized, triple-blind, placebo-controlled clinical trial will evaluate whether adding a 5 mcg/hour transdermal buprenorphine patch to the standard multimodal analgesic regimen reduces postoperative pain in adults undergoing unilateral VATS. Participants will be randomly assigned to receive either transdermal buprenorphine or placebo in addition to standard analgesia. Postoperative pain will be assessed at 24, 48, and 72 hours and 7 days after surgery. Secondary outcomes include opioid rescue requirements, length of hospital stay, postoperative nausea and vomiting, pruritus, and urinary retention.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Clínica DávilaUpdated: Jul 29, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older. [+3]

Known allergy or hypersensitivity to buprenorphine or any component of the trans... [+5]