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
| Type | Name | Description |
|---|---|---|
| DRUG | Gabapentin | |
| DRUG | S-ketamine | |
| DRUG | Lidocaine | |
| DRUG | Droperidol |
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.