Clinical Trials Directory

Trials / Unknown

UnknownNCT00209885

Optimal Multimodal Analgesia in Laparoscopic Cholecystectomy

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
60 (planned)
Sponsor
Hvidovre University Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To test the current standard of care (SOC) treatment for laparoscopic cholecystectomy with a group receiving SOC + additional perioperative analgesics in terms of postoperative abilities, PONV, pain and discharge time from the PACU

Detailed description

Aim of the study: to compare postoperative complaints (PONV, pain, etc) and PACU discharge time between two groups: * A: standard of care (SOC)receiving intraoperative dexamethasone, ondansetron, ketorolac, and general anaesthesia with propofol, remifentanil and cisatracurium * B: SOC + preoperative gabapentin, intraoperative lidocain infusion, s-ketamin and droperidol. Primary endpoints: * postoperative abilities over time * discharge time from PACU according to fixed criteria * consumption of analgesics and antiemetics in the PACU Secondary endpoints: * degree of nursing requirements at the PACU * General tolerability of the regimes

Conditions

Interventions

TypeNameDescription
DRUGGabapentin
DRUGS-ketamine
DRUGLidocaine
DRUGDroperidol

Timeline

Start date
2005-10-01
First posted
2005-09-21
Last updated
2005-09-21

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00209885. Inclusion in this directory is not an endorsement.