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Influence of Epidural Analgesia in Elective Laparoscopic Colorectal Resections

Influence of Epidural Analgesia in Elective Laparoscopic Colorectal Resections

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00512395
Enrollment
75
Registered
2007-08-07
Start date
2004-11-30
Completion date
2007-01-31
Last updated
2024-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

Keywords

laparoscopic colorectal surgery, epidural analgesia, pain score, postoperative ileus

Brief summary

Epidural anaesthesia in open surgery is a effective method for analgesia and has a positive effect on postoperative resolution of ileus. In laparoscopic surgery, the role of epidural surgery is not established. This prospective observational trial evaluates the effect of epidural analgesia in patients undergoing elective, laparoscopic colorectal surgery.

Detailed description

All patients with elective, laparoscopic colorectal resection between November 2004 and January 2007 were included in the trial. The decision for epidural analgesia was made by the anaesthetist and the patient. Contraindications were previous back surgery, coagulopathy, severe spondylarthrosis and refusal by the patient as contraindications. Primary outcome was subjective feeling postoperatively, assessed with a VAS for pain and cramps and amount of analgesics used. Secondary outcomes were duration of postoperative bowel dismotility (first flatus, first defecation, first solid food intake) and general and specific morbidity.

Interventions

DRUGepidural analgesia (Duracain/Fentanyl/Naropin)

naropin 0.3% or duracain 0.125% + Fentanyl via epidural catheter 4-12 ml/h

Sponsors

Triemli Hospital
CollaboratorOTHER
University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* elective laparoscopic colorectal resection

Exclusion criteria

* emergency surgery * preoperatively planned stoma formation

Design outcomes

Primary

MeasureTime frame
pain (VAS), cramps (VAS) and quantity of analgesics8 days

Secondary

MeasureTime frame
duration of postoperative ileus morbidity6 months

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026